Submitted Successfully!
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Ver. Summary Created by Modification Content Size Created at Operation
1
Alexandra Lindsey Djomkam Zune
 + 2729 word(s) 2729 2021-12-06 02:58:24 |
2 revised
Camila Xu
 -109 word(s) 2620 2021-12-20 03:01:16 |

Video Upload Options

Do you have a full video?
Send video materials Upload full video

Confirm

Are you sure to Delete?
Yes No
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Djomkam Zune, A.L.; Olwal, C. Pathogen-Induced Epigenetic Modifications in Cancer in Africa. Encyclopedia. Available online: https://encyclopedia.pub/entry/17308 (accessed on 11 December 2023).
Djomkam Zune AL, Olwal C. Pathogen-Induced Epigenetic Modifications in Cancer in Africa. Encyclopedia. Available at: https://encyclopedia.pub/entry/17308. Accessed December 11, 2023.
Djomkam Zune, Alexandra Lindsey, Charles Olwal. "Pathogen-Induced Epigenetic Modifications in Cancer in Africa" Encyclopedia, https://encyclopedia.pub/entry/17308 (accessed December 11, 2023).
Djomkam Zune, A.L., & Olwal, C.(2021, December 20). Pathogen-Induced Epigenetic Modifications in Cancer in Africa. In Encyclopedia. https://encyclopedia.pub/entry/17308
Djomkam Zune, Alexandra Lindsey and Charles Olwal. "Pathogen-Induced Epigenetic Modifications in Cancer in Africa." Encyclopedia. Web. 20 December, 2021.
Pathogen-Induced Epigenetic Modifications in Cancer in Africa
Edit
This entry is adapted from the peer-reviewed paper 10.3390/cancers13236051

Cancer remains a global burden with multiple causality. Over the years, studies have linked various infectious pathogens with various cancer. Nonetheless, precise mechanism(s) by which pathogens induce or enhance cancer development remains largely obscure. Since cancers are almost invariably associated with genetic alterations, pathogen-induced cancers are likely to be linked with genetic alterations, including epigenetic modification, a change in gene expression without changes in the DNA sequences. Indeed, studies have reported associations between some infectious pathogens can induce epigenetic changes. This implies that pathogens could be involved in cancer development through the modification of host epigenetic factors. With the high burden of infectious pathogens, Africa is at a higher risk of pathogen-mediated cancers. To tame a potential rise of such cancers, there is the need for thorough understanding of the role of tropical infectious pathogens in regulating epigenetic modifications that could be associated with cancer development.

epigenetics tropical pathogens cancer

1. Introduction

Globally, an estimated 19.3 million new cancer cases and almost 10.0 million cancer deaths occurred in 2020 alone. It is projected that by 2040, the burden will rise by 47%. The relative expected magnitude of the increase is most striking in low Human Development Index countries, like Africa, where the burden is likely to rise by 95% [1]. Many of those cases are preventable or treatable at early stages. However, achieving early cancer diagnosis and efficient treatment remains challenging owing to the multiple causalities of the disease and the high infrastructural costs [2] required for cancer diagnosis and management.
Infectious pathogens are a major cause of cancer, especially in low-and middle-income countries, which are ill-equipped to manage the disease. Therefore, the focus should be directed towards the prevention of infections, as this could reduce the development of pathogen-related cancers. It is estimated that in 2018, 2.2 million out of a total of 18 million new cancer cases worldwide were caused by infectious pathogens [3]. In low-income countries mostly in Africa, over 60% of diseases are attributed to infectious pathogens in contrast to high-income countries where less than 5% of diseases are linked to pathogens [4]. The proportion of infection-mediated cancers varies greatly by geographical region [5]. In Africa, 24.5% of cancers are attributed to infectious pathogens [6]. This may be an underestimation considering the limited cancer diagnosis infrastructure in most African countries. 
The involvement of infectious pathogens in carcinogenesis poses a serious threat to the fight against cancer, especially in tropical regions, which have a disproportionately high burden of infectious pathogens. Africa harbors several tropical pathogens, including Plasmodium spp., Leishmania, Schistosoma spp., Trypanosoma spp., Brugia spp., Dengue virus, Chikungunya virus, Wuchereria bancrofti and Onchocerca volvulus. Generally, the etiological role of many of these pathogens in carcinogenesis remains unclear. Several studies have suggested that Helicobacter pylori and Human papillomavirus (HPV) involved in gastric cancer and cervical cancer, respectively, induce carcinogenesis by altering gene expression through epigenetic mechanisms (reviewed in [7]). Furthermore, some of the endemic tropical pathogens, such as S. mansoni [8], O. volvulus [9] and P. falciparum [10], induce inflammation, a key driver of carcinogenesis (reviewed in [11]). Due to their unique diets and lifestyle, Africans tend to have a distinct set of microbiomes [12]. The increasing evidence of microbiome-associated cancers via alteration of the local immune system, systemic deregulation and dysregulation of antitumor immunity [13] suggest that Africans may be at elevated risk of pathogen-associated cancers. Detailed studies aimed at understanding the precise role of tropical pathogens in cancer development could inform on cancer prevention, early diagnosis and pharmacogenomically aided therapy.

2. Epigenetics in Cancer Development and Progression

Epigenetics is a term that describes reversible heritable changes in gene expression without variations in the DNA sequence [14]. Epigenetic deregulation has been recognized as a key player in carcinogenesis [15][16][17]. Observed epigenetic alterations include changes in DNA methylation, histone modifications, and nucleosome positioning [18]. Changes in the epigenome disrupt gene regulation, resulting in cancer-promoting gene expression patterns. Known epigenetic mutations include genome-wide hypomethylation and regional hypermethylation, particularly in promoter-associated CpG islands [19][20][21], universal changes in histone modification marks [21][22] and deregulation of non-coding RNAs [21][23][24].
Adding to the growing knowledge on epigenetics and its role in cancer biology, several studies have demonstrated how deregulation in different epigenetic mechanisms is associated with cancer [25][26][27][28]. It was also demonstrated that the epigenetic alterations leading to carcinogenesis were caused by infectious pathogens; for instance, a proposed mechanism of gastric carcinogenesis by H. pylori is the silencing of miR-490-3p, which reactivates the Chromatin Remodeler, SMARCD1 [29]. Moreover, higher methylation rates of RARbeta2 and APC genes have been observed in Schistosoma-associated bladder cancer compared to non-Schistosoma bladder cancer patients [30].
DNA methylation changes, which involve both hypomethylation and hypermethylation, have received the most attention in epigenetic studies, as aberrations in this modification are common in virtually all cancers [31]. In cancerous cells, DNA hypermethylation has mostly been reported at promoter CpG islands of key genes involved in processes such as cell cycle regulation, DNA repair, apoptosis and differentiation [32]. Moreover, high-throughput analyses of genome-wide DNA methylation have demonstrated distinct epigenetic signatures that correlate with tumor stage and type are reproducibly found in nearly all cases of specific types of cancers [20][33].
Histone modification changes in cancers are less well understood compared to DNA methylation changes. Histone modification enzymes have been shown to exhibit distinct patterns of expression depending on the tissue of origin and can discriminate tumors from their matched normal tissues, clustering them according to cell type [34]. This indicates that abnormal expression of histone modification enzymes is involved in cancer-specific neoplastic transformation [34].
Histone mutations have recently been associated with various cancers. For example, mutations in histone H3 have been reported with high genetic penetrance in rare pediatric gliomas and sarcomas [35][36][37]. These histone mutations have led to the coining of the term “oncohistones”, with several mutations being associated with cancers. For instance, oncohistone H3K27M and H3G34V/R have been identified in diffuse intrinsic pontine gliomas and pediatric glioblastomas, respectively [35][36]. Other studies have shown that the histone H3 variant H3.3 is modified at lysine 36 (H3.3K36M) in 95% of chondroblastomas and at glycine 34 (H3.3G34W/L) in 92% of giant cell tumors of the bone [37]. Oncohistones have also been observed in diffuse large B-cell lymphomas (histone H1), head and neck cancers (H3K36M) and carcinosarcomas (H2A and H2B) [38][39][40]. In some cases, the histone mutations are found to be the only recurrent mutation identified in the tumor, suggesting that they are not only associated with cancer development but also act as initiators [35]. A distinct feature of these common oncohistone mutations is their occurrence at or near key regulatory post-translational modifications in the histone tails, implying a potential interference with the ‘reading’, ‘writing’ and/or ‘erasing’ of these regulatory marks [41].
The frequent genetic alterations in epigenome regulating genes suggest their centrality in carcinogenesis. As shown in Figure 1, our analysis of a few epigenetic regulating genes, such as SETD2, HDAC1, TET2 and EZH2, using The Cancer Genome Atlas (TCGA) Pan-Cancer dataset on cBioPortal for Cancer Genomics (https://www.cbioportal.org/, accessed on 8 November 2021) revealed that these regulatory genes are frequently altered in different cancer types. Thus providing supporting evidence implicating epigenetic regulation as a mechanism underlying tumor development and progression.
Cancers 13 06051 g001 550
Figure 1. Genetic alteration in epigenetic regulating genes across various tumor types. TCGA Pan cancer data from 32 studies were analyzed on cBioPortal for Cancer Genomics. The bars represent the genetic alteration (mutations, amplifications, deep deletions, etc.) frequencies of TET2, SETD2, EZH2 and HDAC1 across different cancers. The analysis was performed as detailed previously [42][43].
Non-coding RNAs play an integral role in gene expression regulation. Their deregulation as a result of amplification, deletions and mutations as well as through other regulator genes have been associated with a growing number of cancers through aberrant functioning of their specific targets [44]. Non-coding RNAs can act as oncogenes or tumor-suppressors. In chronic lymphocytic leukemia (CLL) patients, deletion at the 13q14 region that encodes miR-15 and miR-16 is common [45]. The miR-15 and miR-16 miRNAs are implicated in apoptosis through their targeting of B-cell lymphoma 2 (BCL-2) [45]. Another example of non-coding epigenetic regulation is seen in B cell lymphoma, where the miR-17~92 cluster (13q31-q32) is amplified and acts with MYC to promote tumor development in hematopoietic malignancies [46].

3. Overview of Cancer Epigenetic Studies Conducted in Populations of African Descent

Africa is a region of considerable genetic, cultural, geographical and phenotypic diversity [47][48]. These variable factors among Africans, especially genetic, environmental and dietary are critical for understanding the genetic risk factors for disease, gene-environment interactions and epigenetic basis of human diseases [47]. However, most studies have focused on non-African residents; hence, the interplay between these factors and human genetic diseases is scanty. Studying the epigenome is important, as alterations in epigenetic processes drive many diseases, including cancer [31].
Ethnic disparities in cancer measures such as incidence, prevalence, mortality, survival and morbidity have been reported and epigenetic modifications could be contributing factors. However, while studies on the epigenetic basis of different types of cancers have mainly focused on mostly Caucasians and African Americans to a lesser extent [49] as summarized in Table 1, cancer epigenetics studies on people residing in Africa are largely lacking.
Table 1. Epigenetic modifications in African Americans and the genes implicated.
Type of Cancer Epigenetic
Modification		 Genes/miRNA
Involved		 Differences between African
Americans and Caucasians		 Link with Disease
Progression		 References
Prostate Hypermethylation CD44, GSTP1 Higher frequency of CD44
hypermethylation in African Americans		 Not indicated [50]
Hypermethylation Nkx2-5, TIMP3 AR,
RARβ2, SPARC		 Higher methylation in African
Americans		 Yes [51]
Hypermethylated miR-152 Higher methylation in African
Americans		 Yes [52]
Colorectal Hypermethylation CHL1, NELL1, GDF1,
ARHGEF4, ITGA4		 Higher methylation in African
Americans		 Not indicated [53]
Hypermethylation miR-9, miR-124, miR-137,
miR-548, miR-663,
miR-2682, miR-6130		 Higher methylation in African
Americans		 Not indicated [53]
Breast Hypermethylation CDH13, HIN-1, TWIST,
RAR-β, RASSF1A		 Higher methylation in African
Americans		 Not indicated [54]
Thyroid miRNA Upregulation miR-31, miR-221 Upregulated in Caucasians
downregulated in African Americans		 Yes [55]
Endometrial RNA Down-regulation miR-337 Downregulated in Caucasians
compared with African Americans		 Not indicated [56]
Lung Hypomethylation SHISA4, RAD1 Decreased DNA methylation in African
Americans		 Yes [57]
Africans also have an environment that harbors many infectious pathogens capable of driving cancer [58]. Hence, it is likely that African populations have both genetic and environmental influences on the methylome [49]. Consequently, resident Africans are more exposed to pathogenic infections compared to non-resident Africans. However, knowledge on the role of epigenetics in cancer in Africa is usually drawn from studies conducted among African Americans, which should not be extrapolated to native Africans due to admixture [59][60] and the higher genetic diversity in extant Africans. Epigenetic therapy is a rapidly advancing field of cancer research, since targeting epigenetic aberrations offers remarkable promise as a potential anti-cancer therapy, given the reversible nature of epigenetic changes [61]. Therefore, the lack of cancer epigenetics studies in Africa might have negative implications for people residing in Africa, as treatment development from studies in other ethnicities might not be effective for people of African descent. This calls for African-tailored cancer-related epigenetic studies to inspire African-specific cancer diagnostics and therapies. Advances in scientific research approaches, such as sequencing technologies, enabling the characterization of tumor phenotypes on a large scale, have highlighted epigenetic changes as a hallmark of cancer [61] and are promising solutions to overcome longstanding limitations in cancer epigenetics research [62]. While sequencing technologies are being applied in cancer epigenetic research in other parts of the world, their usage in Africa is relatively low, partly due to limited resources and technical know-how [63]. Therefore, more initiatives such as the Human Heredity and Health in Africa (H3Africa) consortium, a platform for collaboration and capacity building, should be created to focus on cancer epigenetics in Africa. Such initiatives will be invaluable in generating funds, training younger researchers and capacity building in cancer epigenetics research and development of cancer diagnostics and therapeutics.

4. Correlating the Prevalence of Tropical Pathogens and Cancer Prevalence

Besides causing infectious diseases, the role of infectious agents in non-communicable diseases including cancers is increasingly being appreciated. Currently, infections collectively account for 25–50% of all human cancers [64].
Infectious carcinogens affecting humans span all classes of microbial pathogens—viruses, bacteria, fungi and parasites. Among viruses, the Epstein-Barr virus (EBV), hepatitis C virus (HCV), hepatitis B virus (HBV), Kaposi’s sarcoma herpesvirus (KSHV), human immunodeficiency virus type-1 (HIV-1), human T cell lymphotropic virus type-1 (HTLV-1) and high-risk HPV (HR-HPV) genotypes are well-linked to cancer [65]. Notably, HR-HPV, HBV and HCV accounted for 690,000, 360,000 and 160,000 new cancer cases worldwide, respectively, in 2018 [3]. Most of these viral pathogens have been reported in Africa. For instance, the prevalence of HBV and HCV among the general population in the World Health Organization’s African Region is estimated at 7.5% and 1.0%, respectively, while for HIV, the prevalence is 3.6% among adults [66][67]. In Africa, EBV has been associated with endemic Burkitt’s lymphoma and other cancers such as nasopharyngeal carcinoma [68].
There are relatively fewer bacteria known to cause cancer. Thus far, Helicobacter pylori, a gastric ulcer-associated pathogen, is the only bacterium that has been clearly shown to be oncogenic. H. pylori causes both gastric cardia and gastric non-cardia adenocarcinoma [69], as well as non-Hodgkin lymphoma of gastric location [70]. Globally, H. pylori was the leading cause of infection-related cancer in 2018, being responsible for 810,000 new cancer cases [3]. Limited epidemiological evidence indicates a sexually transmitted bacterium, Chlamydia trachomatis, in ovarian cancer [71] and as a cofactor of HPV-associated cervical cancer [72]. This evidence is further supported by the extensive host DNA damage and depletion of the tumor suppressor p53 observed during Chlamydia infection [73]. Furthermore, a nationwide cohort study in Taiwan has associated genitourinary tuberculosis with urothelial cancer [74]. Together, these observations underscore the need for more studies to explore the role of bacteria in human cancers.
Three parasites, namely, Schistosoma haematobium, Opisthorchis viverrini and Clonorchis sinensis, are also considered oncogenic pathogens [75]. A link between S. haematobium and bladder cancer has long been established [76]. Globally, a total of 550,000 new cases of bladder cancer were reported in 2018 with S. haematobium accounting for about 1.1% [3]. The role of S. haematobium in bladder cancer is likely to be higher in Africa, where about 90% of those requiring treatment globally for schistosomiasis reside [77].
In addition to S. haematobium, three foodborne liver flukes, Opisthorchis viverrini, Opisthorchis felineus and Clonorchis sinensis, have been linked to hepatic cancers [78][79][80]. Although these parasites have not been reported in Africa, chronic infection by these parasites has been linked to cholangiocarcinoma, a bile duct cancer, in other parts of the world [81]. In 2018, O. viverrini and C. sinensis together accounted for 3500 (2.7%) of the 130,000 new cases of cholangiocarcinoma reported globally [3].
Aspergillus flavus, a fungus that is more prevalent in tropical regions, produces mycotoxins, particularly B1 aflatoxins, which are known to cause hepatocellular carcinoma (HCC) [82][83], as well as lung cancers [84]. Similarly, two other mycotoxins, ochratoxin and sterigmatocystin produced by fungi of the genus Aspergillus, have been implicated in some malignancies such as breast and testicular cancers [85]. In addition, a recent study by Aykut et al. demonstrated that in animal models and humans, mycological dysbiosis of the gut favoring infiltration of the pancreas by Malassezia species promotes pancreatic ductal adenocarcinoma [86]. Collectively, these findings highlight the role of fungi or their metabolites in many malignancies.
The involvement of infectious pathogens in carcinogenesis poses a serious threat to cancer prevention, especially in tropical climates, where the burden of infection is high. Unfortunately, many aspects of this involvement such as the mechanism of infection-induced carcinogenesis, have not been elucidated. Hence, further studies are needed to unravel the links between infection and cancers to help accelerate diagnostics, drug and vaccine development.

5. Conclusions

Despite the steady surge of cancers in Africa, significant progress in curbing the disease is still far from realization. Whereas epigenetic studies are a promising avenue for cancer detection and management, there is a significant paucity of data from the African continent. Infectious pathogens mediate epigenetic alterations associated with carcinogenesis, and Africa carries the highest burden of infections. This suggests a predisposition to pathogen-induced epigenetic changes that may lead to cancer development among native Africans. Thus, detailed studies on the patterns of epigenetic deregulation, as well as the role of tropical pathogens in infection-associated cancer in Africa are crucial. Such studies are likely to identify targets for African-specific prevention, diagnosis and therapeutic strategies that could ultimately tame the rising tide of cancer cases and mortalities in Africa.

References

  1. Sung, H.; Ferlay, J.; Siegel, R.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249.
  2. Rebbeck, T.R. Cancer in Sub-Saharan Africa. Science 2020, 367, 27–28.
  3. de Martel, C.; Georges, D.; Bray, F.; Ferlay, J.; Clifford, G.M. Global Burden of Cancer Attributable to Infections in 2018: A Worldwide Incidence Analysis. Lancet Glob. Health 2020, 8, e180–e190.
  4. Roser, M.; Ritchie, H. Burden of Disease. Available online: https://ourworldindata.org/burden-of-disease (accessed on 8 November 2021).
  5. Wild, C.P.; Weiderpass, E.; Stewart, B.W. World Cancer Report 2020: Cancer Research for Cancer Prevention; International Agency for Research and Cancer: Lyon, France, 2020; Volume 199.
  6. Parkin, D.M.; Hämmerl, L.; Ferlay, J.; Kantelhardt, E.J. Cancer in Africa 2018: The Role of Infections. Int. J. Cancer 2020, 146, 2089–2103.
  7. Hattori, N.; Ushijima, T. Epigenetic Impact of Infection on Carcinogenesis: Mechanisms and Applications. Genome Med. 2016, 8, 10.
  8. Dewals, B.; Hoving, J.C.; Horsnell, W.G.C.; Brombacher, F. Control of Schistosoma Mansoni Egg-Induced Inflammation by IL-4-Responsive CD4(+)CD25(-)CD103(+)Foxp3(-) Cells Is IL-10-Dependent. Eur. J. Immunol. 2010, 40, 2837–2847.
  9. Gillette-Ferguson, I.; Hise, A.G.; Sun, Y.; Diaconu, E.; McGarry, H.F.; Taylor, M.J.; Pearlman, E. Wolbachia- and Onchocerca Volvulus-Induced Keratitis (River Blindness) Is Dependent on Myeloid Differentiation Factor 88. Infect. Immunol. 2006, 74, 2442–2445.
  10. Orengo, J.M.; Leliwa-Sytek, A.; Evans, J.E.; Evans, B.; van de Hoef, D.; Nyako, M.; Day, K.; Rodriguez, A. Uric Acid Is a Mediator of the Plasmodium Falciparum-Induced Inflammatory Response. PLoS ONE 2009, 4, e5194.
  11. Coussens, L.M.; Werb, Z. Inflammation and Cancer. Nature 2002, 420, 860–867.
  12. Brewster, R.; Tamburini, F.B.; Asiimwe, E.; Oduaran, O.; Hazelhurst, S.; Bhatt, A.S. Surveying Gut Microbiome Research in Africans: Toward Improved Diversity and Representation. Trends Microbiol. 2019, 27, 824–835.
  13. Rao Malla, R.; Marni, R.; Kumari, S.; Chakraborty, A.; Lalitha, P. Microbiome Assisted Tumor Microenvironment: Emerging Target of Breast Cancer. Clin. Breast Cancer 2021, in press.
  14. Cheng, Y.; He, C.; Wang, M.; Ma, X.; Mo, F.; Yang, S.; Han, J.; Wei, X. Targeting Epigenetic Regulators for Cancer Therapy: Mechanisms and Advances in Clinical Trials. Signal Transduct. Target. Ther. 2019, 4, 62.
  15. Garraway, L.A.; Lander, E.S. Lessons from the Cancer Genome. Cell 2013, 153, 17–37.
  16. Jones, P.A.; Issa, J.P.J.; Baylin, S. Targeting the Cancer Epigenome for Therapy. Nat. Rev. Genet. 2016, 17, 630–641.
  17. Dawson, M.A. The Cancer Epigenome: Concepts, Challenges, and Therapeutic Opportunities. Science 2017, 355, 1147–1152.
  18. Portela, A.; Esteller, M. Epigenetic Modifications and Human Disease. Nat. Biotechnol. 2010, 28, 1057.
  19. Baylin, S.B.; Jones, P.A. Epigenetic Determinants of Cancer. Cold Spring Harb. Perspect. Biol. 2016, 8, a019505.
  20. Fernandez, A.F.; Assenov, Y.; Martin-Subero, J.I.; Balint, B.; Siebert, R.; Taniguchi, H.; Yamamoto, H.; Hidalgo, M.; Tan, A.C.; Galm, O.; et al. A DNA Methylation Fingerprint of 1628 Human Samples. Genome Res. 2012, 22, 407–419.
  21. Kanwal, R.; Gupta, S. Epigenetic Modifications in Cancer. Clin. Genet. 2012, 81, 303–311.
  22. Hosseini, A.; Minucci, S. Alterations of histone modifications in cancer. In Epigenetics in Human Disease, 2nd ed.; Tollefsbol, T., Ed.; Academic Press: Waltham, MA, USA, 2018; pp. 141–217.
  23. Esteller, M. Non-Coding RNAs in Human Disease. Nat. Rev. Genet. 2011, 12, 861–874.
  24. Liz, J.; Esteller, M. LncRNAs and MicroRNAs with a Role in Cancer Development. Biochim. Biophys. Acta BBA—Gen. Regul. Mech. 2016, 1859, 169–176.
  25. Yang, J.H.; Lin, L.K.; Zhang, S. Epigenetic Silencing of MicroRNA-335 Contributes to Nasopharyngeal Carcinoma Metastasis. Am. J. Otolaryngol. Head Neck Med. Surg. 2020, 41, 102302.
  26. Law, C.-T.; Wei, L.L.; Tsang, F.H.; Xu, I.M.; Lai, R.K.; Ho, D.W.; Lee, J.M.; Wong, C.C.; Ng, I.O.; Wong, J.C.; et al. Chromatin Remodeler HELLS Is an Epigenetic Driver for Hepatocellular Carcinoma Progression. In Proceedings of the Cancer Research, American Association for Cancer Research (AACR), Washington, DC, USA, 1–5 April 2017; Volume 77, p. 1022.
  27. Ward, A.K.; Mellor, P.; Smith, S.E.; Kendall, S.; Just, N.A.; Vizeacoumar, F.S.; Sarker, S.; Phillips, Z.; Alvi, R.; Saxena, A.; et al. Epigenetic Silencing of CREB3L1 by DNA Methylation Is Associated with High-Grade Metastatic Breast Cancers with Poor Prognosis and Is Prevalent in Triple Negative Breast Cancers. Breast Cancer Res. 2016, 18, 12.
  28. Kim, K.H.; Roberts, C.W.M. Targeting EZH2 in Cancer. Nat. Med. 2016, 22, 128–134.
  29. Shen, J.; Xiao, Z.; Wu, W.K.K.; Wang, M.H.; To, K.F.; Chen, Y.; Yang, W.; Li, M.S.M.; Shin, V.Y.; Tong, J.H.; et al. Epigenetic Silencing of MiR-490-3p Reactivates the Chromatin Remodeler SMARCD1 to Promote Helicobacter Pylori-Induced Gastric Carcinogenesis. Cancer Res. 2015, 75, 754–765.
  30. Eissa, S.; Swellam, M.; El-Khouly, I.M.; Kassim, S.K.; Shehata, H.; Mansour, A.; Esmat, M.; Nossier, A.I.; Hamdy, M.A.; Awad, N.M.; et al. Aberrant Methylation of RARβ2and APC Genes in Voided Urine as Molecular Markers for Early Detection of Bilharzial and Nonbilharzial Bladder Cancer. Cancer Epidemiol. Biomark. Prev. 2011, 20, 1657–1664.
  31. Sharma, S.; Kelly, T.K.; Jones, P.A. Epigenetics in Cancer. Carcinogenesis 2009, 31, 27–36.
  32. Pfeifer, G.P. Defining Driver DNA Methylation Changes in Human Cancer. Int. J. Mol. Sci. 2018, 19, 1166.
  33. Hao, X.; Luo, H.; Krawczyk, M.; Wei, W.; Wang, W.; Wang, J.; Flagg, K.; Hou, J.; Zhang, H.; Yi, S.; et al. DNA Methylation Markers for Diagnosis and Prognosis of Common Cancers. Proc. Natl. Acad. Sci. USA 2017, 114, 7414–7419.
  34. Özdağ, H.; Teschendorff, A.E.; Ahmed, A.A.; Hyland, S.J.; Blenkiron, C.; Bobrow, L.; Veerakumarasivam, A.; Burtt, G.; Subkhankulova, T.; Arends, M.J.; et al. Differential Expression of Selected Histone Modifier Genes in Human Solid Cancers. BMC Genom. 2006, 7, 90.
  35. Schwartzentruber, J.; Korshunov, A.; Liu, X.-Y.; Jones, D.T.W.; Pfaff, E.; Jacob, K.; Sturm, D.; Fontebasso, A.M.; Quang, D.-A.K.; Tönjes, M.; et al. Driver Mutations in Histone H3.3 and Chromatin Remodelling Genes in Paediatric Glioblastoma. Nature 2012, 482, 226–231.
  36. Behjati, S.; Tarpey, P.S.; Presneau, N.; Scheipl, S.; Pillay, N.; Van Loo, P.; Wedge, D.C.; Cooke, S.L.; Gundem, G.; Davies, H.; et al. Distinct H3F3A and H3F3B Driver Variants Define Chondroblastoma and Giant Cell Tumour of Bone. Nat. Genet. 2013, 45, 1479–1482.
  37. Wu, G.; Broniscer, A.; McEachron, T.A.; Lu, C.; Paugh, B.S.; Becksfort, J.; Qu, C.; Ding, L.; Huether, R.; Parker, M.; et al. Somatic Histone H3 Alterations in Paediatric Diffuse Intrinsic Pontine Gliomas and Non-Brainstem Glioblastomas. Nat. Genet. 2012, 44, 251–253.
  38. Lohr, J.G.; Stojanov, P.; Lawrence, M.S.; Auclair, D.; Chapuy, B.; Sougnez, C.; Cruz-Gordillo, P.; Knoechel, B.; Asmann, Y.W.; Slager, S.L.; et al. Discovery and Prioritization of Somatic Mutations in Diffuse Large B-Cell Lymphoma (DLBCL) by Whole-Exome Sequencing. Proc. Natl. Acad. Sci. USA 2012, 109, 3879–3884.
  39. Papillon-Cavanagh, S.; Lu, C.; Gayden, T.; Mikael, L.G.; Bechet, D.; Karamboulas, C.; Ailles, L.; Karamchandani, J.; Marchione, D.M.; Garcia, B.A.; et al. Impaired H3K36 Methylation Defines a Subset of Head and Neck Squamous Cell Carcinomas. Nat. Genet. 2017, 49, 180–185.
  40. Zhao, S.; Bellone, S.; Lopez, S.; Thakral, D.; Schwab, C.; English, D.P.; Black, J.; Cocco, E.; Choi, J.; Zammataro, L.; et al. Mutational Landscape of Uterine and Ovarian Carcinosarcomas Implicates Histone Genes in Epithelial–Mesenchymal Transition. Proc. Natl. Acad. Sci. USA 2016, 113, 12238–12243.
  41. Lewis, P.W.; Müller, M.M.; Koletsky, M.S.; Cordero, F.; Lin, S.; Banaszynski, L.A.; Garcia, B.A.; Muir, T.W.; Becher, O.J.; Allis, C.D. Inhibition of PRC2 Activity by a Gain-of-Function H3 Mutation Found in Pediatric Glioblastoma. Science 2013, 340, 857–861.
  42. Gao, J.; Aksoy, B.A.; Dogrusoz, U.; Dresdner, G.; Gross, B.; Sumer, S.O.; Sun, Y.; Jacobsen, A.; Sinha, R.; Larsson, E.; et al. Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the CBioPortal. Sci. Signal. 2013, 6, pl1.
  43. Cerami, E.; Gao, J.; Dogrusoz, U.; Gross, B.E.; Sumer, S.O.; Aksoy, B.A.; Jacobsen, A.; Byrne, C.J.; Heuer, M.L.; Larsson, E.; et al. The cBio cancer genomics portal: An open platform for exploring multidimensional cancer genomics data. Cancer Discov. 2012, 2, 401–404.
  44. Ferreira, H.J.; Esteller, M. Non-Coding RNAs, Epigenetics, and Cancer: Tying It All Together. Cancer Metastasis Rev. 2018, 37, 55–73.
  45. Calin, G.A.; Dumitru, C.D.; Shimizu, M.; Bichi, R.; Zupo, S.; Noch, E.; Aldler, H.; Rattan, S.; Keating, M.; Rai, K.; et al. Frequent Deletions and Down-Regulation of Micro- RNA Genes MiR15 and MiR16 at 13q14 in Chronic Lymphocytic Leukemia. Proc. Natl. Acad. Sci. USA 2002, 99, 15524–15529.
  46. Lin, S.; Gregory, R. MicroRNA Biogenesis Pathways in Cancer. Nat. Rev. Cancer 2015, 15, 321–333.
  47. Tishkoff, S.A.; Reed, F.A.; Friedlaender, F.R.; Ranciaro, A.; Froment, A.; Hirbo, J.B.; Awomoyi, A.A.; Bodo, J.; Doumbo, O.; Ibrahim, M.; et al. The Genetic Structure and History of Africans and African Americans. Science 2010, 324, 1035–1044.
  48. Reed, F.A.; Tishkoff, S.A. African Human Diversity, Origins and Migrations. Curr. Opin. Genet. Dev. 2006, 16, 597–605.
  49. Hobbs, A.; Ramsay, M. Epigenetics and the Burden of Noncommunicable Disease: A Paucity of Research in Africa. Epigenomics 2015, 7, 627–639.
  50. Woodson, K.; Hayes, R.; Wideroff, L.; Villaruz, L.; Tangrea, J. Hypermethylation of GSTP1, CD44, and E-Cadherin Genes in Prostate Cancer among US Blacks and Whites. Prostate 2003, 55, 199–205.
  51. Kwabi-Addo, B.; Wang, S.; Chung, W.; Jelinek, J.; Patierno, S.R.; Wang, B.D.; Andrawis, R.; Lee, N.H.; Apprey, V.; Issa, J.P.; et al. Identification of Differentially Methylated Genes in Normal Prostate Tissues from African American and Caucasian Men. Clin. Cancer Res. 2010, 16, 3539–3547.
  52. Theodore, S.C.; Davis, M.; Zhao, F.; Wang, H.; Chen, D.; Rhim, J.; Dean-Colomb, W.; Turner, T.; Ji, W.; Zeng, G.; et al. MicroRNA Profiling of Novel African American and Caucasian Prostate Cancer Cell Lines Reveals a Reciprocal Regulatory Relationship of MiR-152 and DNA Methyltranferase 1. Oncotarget 2014, 5, 3512–3525.
  53. Wang, X.; Ji, P.; Zhang, Y.; LaComb, J.F.; Tian, X.; Li, E.; Williams, J.L. Aberrant DNA Methylation: Implications in Racial Health Disparity. PLoS ONE 2016, 11, e0153125.
  54. Mehrotra, J.; Ganpat, M.M.; Kanaan, Y.; Fackler, M.J.; McVeigh, M.; Lahti-Domenici, J.; Polyak, K.; Argani, P.; Naab, T.; Garrett, E.; et al. Estrogen Receptor/Progesterone Receptor-Negative Breast Cancers of Young African-American Women Have a Higher Frequency of Methylation of Multiple Genes than Those of Caucasian Women. Clin. Cancer Res. 2004, 10, 2052–2057.
  55. Seema Sethi, R.S. Differential Expression of MicroRNAs in Papillary Thyroid Carcinoma and Their Role in Racial Disparity. J. Cancer Sci. Ther. 2015, 7, 145–154.
  56. Maxwell, G.L.; Shoji, Y.; Darcy, K.; Litzi, T.; Berchuck, A.; Hamilton, C.A.; Conrads, T.P.; Risinger, J.I. MicroRNAs in Endometrial Cancers from Black and White Patients. Am. J. Obstet. Gynecol. 2015, 212, 191.e1–191.e10.
  57. McHayle, A.; Boles, A.; Diarra, L.; Mitchell, K.A. Epigenetics, Regulation of Cancer Immunotherapy Response Genes, and Race: A Comparison of DNA Methylation in Non-Small Cell Lung Cancers from African Americans and European Americans (Abstract). Am. Assoc. Cancer Res. 2018, 78, 3325.
  58. Vandeven, N.; Nghiem, P. Pathogen-Driven Cancers and Emerging Immune Therapeutic Strategies. Cancer Immunol. Res. 2014, 2, 9–14.
  59. Xia, Y.Y.; Ding, Y.B.; Liu, X.Q.; Chen, X.M.; Cheng, S.Q.; Li, L.B.; Ma, M.F.; He, J.L.; Wang, Y.X. Racial/Ethnic Disparities in Human DNA Methylation. Biochim. Biophys. Acta Rev. Cancer 2014, 1846, 258–262.
  60. Campbell, M.C.; Tishkoff, S.A. African Genetic Diversity: Implications for Human Demographic History, Modern Human Origins, and Complex Disease Mapping. Annu. Rev. Genom. Hum. Genet. 2008, 9, 403–433.
  61. Hillyar, C.; Rallis, K.S.; Varghese, J. Advances in Epigenetic Cancer Therapeutics. Cureus 2020, 12, e11725.
  62. de Vries, J.; Pepper, M. Genomic Sovereignty and the African Promise: Mining the African Genome for the Benefit of Africa. J. Med. Ethics 2012, 38, 474–478.
  63. Ramsay, M. Africa: Continent of Genome Contrasts with Implications for Biomedical Research and Health. FEBS Lett. 2012, 586, 2813–2819.
  64. Knoll, L.J.; Hogan, D.A.; Leong, J.M.; Heitman, J.; Condit, R.C. Pearls Collections: What We Can Learn about Infectious Disease and Cancer. PLoS Pathog. 2018, 14, e1006915.
  65. White, M.K.; Pagano, J.S.; Khalili, K. Viruses and Human Cancers: A Long Road of Discovery of Molecular Paradigms. Clin. Microbiol. Rev. 2014, 27, 463–481.
  66. World Health Organization. Global Hepatitis Report 2017; World Health Organization: Geneva, Switzerland, 2017; pp. 1–83.
  67. WHO. Global Progress Report on HIV, Viral Hepatitis and Sexually Transmitted Infections; World Health Organization: Geneva, Switzerland, 2021; pp. 1–112.
  68. Ayee, R.; Ofori, M.E.O.; Tagoe, E.A.; Languon, S.; Searyoh, K.; Armooh, L.; Bilson-Amoah, E.; Baidoo, K.; Kitcher, E.; Wright, E.; et al. Genotypic Characterization of Epstein Barr Virus in Blood of Patients with Suspected Nasopharyngeal Carcinoma in Ghana. Viruses 2020, 12, 766.
  69. Moss, S.F. The Clinical Evidence Linking Helicobacter pylori to Gastric Cancer. Cell Mol. Gastroenterol. Hepatol. 2017, 3, 183–191.
  70. Cheng, Y.; Xiao, Y.; Zhou, R.; Liao, Y.; Zhou, J.; Ma, X. Prognostic Significance of Helicobacter pylori—Infection in Gastric Diffuse Large B-Cell Lymphoma. BMC Cancer 2019, 19, 842.
  71. Trabert, B.; Waterboer, T.; Idahl, A.; Brenner, N.; Brinton, L.A.; Butt, J.; Coburn, S.B.; Hartge, P.; Hufnagel, K.; Inturrisi, F.; et al. Antibodies against Chlamydia Trachomatis and Ovarian Cancer Risk in Two Independent Populations. J. Natl. Cancer Inst. 2019, 111, 129–136.
  72. Smith, J.S.; Muñoz, N.; Herrero, R.; Eluf-Neto, J.; Ngelangel, C.; Franceschi, S.; Bosch, F.X.; Walboomers, J.M.M.; Peeling, R.W. Evidence for Chlamydia Trachomatis as a Human Papillomavirus Cofactor in the Etiology of Invasive Cervical Cancer in Brazil and the Philippines. J. Infect. Dis. 2002, 185, 324–331.
  73. González, E.; Rother, M.; Kerr, M.C.; Al-Zeer, M.A.; Abu-Lubad, M.; Kessler, M.; Brinkmann, V.; Loewer, A.; Meyer, T.F. Chlamydia Infection Depends on a Functional MDM2-P53 Axis. Nat. Commun. 2014, 5, 5201.
  74. Lien, Y.C.; Wang, J.Y.; Lee, M.C.; Shu, C.C.; Chen, H.Y.; Hsieh, C.H.; Lee, C.H.; Lee, L.N.; Chao, K.M. Urinary Tuberculosis Is Associated with the Development of Urothelial Carcinoma but Not Renal Cell Carcinoma: A Nationwide Cohort Study in Taiwan. Br. J. Cancer 2013, 109, 2933–2940.
  75. Marbjerg, L.H.; Øvrehus, A.L.H.; Johansen, I.S. Schistosomiasis-Induced Squamous Cell Bladder Carcinoma in an HIV-Infected Patient. Int. J. Infect. Dis. 2015, 40, 113–115.
  76. Ishida, K.; Hsieh, M.H. Understanding Urogenital Schistosomiasis-Related Bladder Cancer: An Update. Front. Med. 2018, 5, 223.
  77. WHO Schistosomiasis. Available online: https://www.who.int/news-room/fact-sheets/detail/schistosomiasis (accessed on 10 November 2021).
  78. Kaewpitoon, N.; Kaewpitoon, S.J.; Pengsaa, P.; Sripa, B. Opisthorchis viverrini: The Carcinogenic Human Liver Fluke. World J. Gastroenterol. 2008, 14, 666–674.
  79. Bollati, V.; Fabris, S.; Pegoraro, V.; Ronchetti, D.; Mosca, L.; Deliliers, G.L.; Motta, V.; Bertazzi, P.A.; Baccarelli, A.; Neri, A. Differential repetitive DNA methylation in multiple myeloma molecular subgroups. Carcinogenesis 2009, 30, 1330–1335.
  80. Kim, T.S.; Pak, J.H.; Kim, J.B.; Bahk, Y.Y. Clonorchis sinensis, an Oriental Liver Fluke, as a Human Biological Agent of Cholangiocarcinoma: A Brief Review. BMB Rep. 2016, 49, 590–597.
  81. Sripa, B.; Kaewkes, S.; Sithithaworn, P.; Mairiang, E.; Laha, T.; Smout, M.; Pairojkul, C.; Bhudhisawasdi, V.; Tesana, S.; Thinkamrop, B.; et al. Liver Fluke Induces Cholangiocarcinoma. PLoS Med. 2007, 4, 1148–1155.
  82. Hamid, A.S.; Tesfamariam, S.G.; Zhang, Y.; Zhang, Z.G. Aflatoxin B1-Induced Hepatocellular Carcinoma in Developing Countries: Geographical Distribution, Mechanism of Action and Prevention (Review). Oncol. Lett. 2013, 5, 1087–1092.
  83. Liu, Y.; Wu, F. Global Burden of Aflatoxin-Induced Hepatocellular Carcinoma: A Risk Assessment. Environ. Health Perspect. 2010, 118, 818–824.
  84. Massey, T.E.; Smith, G.B.J.; Tam, A.S. Mechanism of Aflatoxin B1 Lung Tumorigenesis. Exp. Lung Res. 2000, 26, 673–683.
  85. Adam, M.A.A.; Tabana, Y.M.; Musa, K.B.; Sandai, D.A. Effects of Different Mycotoxins on Humans, Cell Genome and Their Involvement in Cancer (Review). Oncol. Rep. 2017, 37, 1321–1336.
  86. Aykut, B.; Pushalkar, S.; Chen, R.; Li, Q.; Abengozar, R.; Kim, J.I.; Shadaloey, S.A.; Wu, D.; Preiss, P.; Verma, N.; et al. The Fungal Mycobiome Promotes Pancreatic Oncogenesis via Activation of MBL. Nature 2019, 574, 264–267.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY)license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Biochemistry & Molecular Biology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Alexandra Lindsey Djomkam Zune
,
Charles Olwal
View Times: 169
Revisions: 2 times (View History)
Update Date: 20 Dec 2021
Table of Contents
    1000/1000
    Hot Most Recent
    Feedback