Implantation-Based Genetic Modeling of BTC: History
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Subjects: Oncology
Contributor:
Yoshitaka Hippo

Biliary tract cancer (BTC) is often refractory to conventional therapeutics and is difficult to diagnose in the early stages. Implantation-based models have recently drawn attention for their convenience, flexibility, and scalability. 

  • genetically engineered mouse
  • biliary tract cancer
  • organoid
  • orthotopic model
  • nude mouse
  • syngeneic
  • hydrodynamic injection
  • implantation

1. Introduction

The biliary system is a network of bile ducts that collect bile produced and secreted by hepatocytes in the liver. The bile ducts merge into the common bile duct (CBD), transporting bile to the duodenum, where it aids the absorption of dietary lipids in the intestine. The gall bladder (GB) is located in the middle of this network. It functions to temporally store bile during the fast state, which in turn is secreted by GB contraction upon food intake. Biliary tract cancer (BTC) is a malignant tumorous cancer that arises from epithelial cells that cover the lumen of the bile duct. It is typically divided into three subtypes (Figure 1) based on anatomical site: intrahepatic cholangiocarcinoma (iCCA), extrahepatic cholangiocarcinoma (eCCA), and gallbladder carcinoma (GBC). While the histological diagnosis for most BTCs is adenocarcinoma, a subset of liver cancer is a biphasic tumor comprising both iCCA and hepatocellular carcinoma (HCC), thereby diagnosed as mixed type [1].
Cancers 13 02292 g001 550
Figure 1. Malignancy of the hepatobiliary system. Anatomical classification of the biliary system (left). The corresponding tumors are listed (right). Biliary tract cancers (BTC) (blue) and liver cancer (black) are not necessarily mutually exclusive.
The major risk factors for BTC include chronic infection with liver fluke and primary sclerosing cholangitis. Other risk factors include chronic liver disease, stones, fibrocystic polycystic disease, chemicals, obesity, aging, and some genetic diseases, suggesting that chronic inflammation in the local biliary tract may be implicated in its pathogenesis [2]. Worldwide, iCCA cases are increasing, and eCCA cases are decreasing. The reasons for this trend remain largely unknown [3][4]. BTC is one of the most devastating cancer types, with a 5-year survival rate of approximately 10% to 30% for all patients and 2% to 3% for patients with metastatic disease. Although biliary intraepithelial neoplasia (BilIN) [5][6] is regarded as a putative pre-cancerous lesion for BTC, it can only be detected by histological examination of the tumors. Non-invasive diagnostic modalities, such as serum biomarkers or imaging, have not been developed. For early stage tumors, surgical resection followed by adjuvant chemotherapy is the first-line therapy to achieve a complete cure. In contrast, patients with advanced or metastatic disease are treated with systemic chemotherapy, radiation therapy, and local therapy, which may lead to palliative care.
Recent genomic analyses have revealed that mutations in tumor protein 53 (TP53), BReast CAncer gene (BRCA), phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA), and KRAS are commonly found in all types of BTC. In contrast, fibroblast growth factor receptor 2 (FGFR2) fusion genes and isocitrate dehydrogenase 1 (IDH1) mutations are preferentially detected in iCCA, protein kinase CAMP-activated catalytic subunit alpha (PRKACA)- and PRKACB-fusion genes in eCCA, and mutations in epidermal growth factor receptor (EGFR), ERBB3, and phosphatase and tensin homolog (PTEN) in GBC [7][8][9][10][11][12][13][14]. Hence, molecular targeted therapies with inhibitors of IDH or FGFR can be considered for patients with iCCA. Radiation therapy and immunotherapy with immune checkpoint inhibitors or chimeric antigen receptor T cell therapy may also be applied, although their efficacy remains elusive. Mouse models, particularly genetically engineered mice (GEM), have been fundamentally important in elucidating the mechanisms underlying BTC development and are a potentially powerful tool for preclinical studies.
Given the recent progress in cancer genome projects and their application to genomic medicine in clinical practice, this work comprehensively reviews the recent progress in mouse BTC models, emphasizing those that recapitulate the whole processes of BTC development by genetic approaches. Although perihilar cholangiocarcinoma (pCCA) is a distinct entity of high clinical relevance, it is not distinguished from eCCA in most genomic studies, and no mouse model has been developed for pCCA. Therefore, we adopted this classification of BTC in this review and excluded hepatocellular carcinoma (HCC) models unless the induced tumors were mixed with iCCA. Similarly, other BTC models [15][16][17] with patient-derived xenografts in immunodeficient mice, or in vivo mouse models based on the liver damage caused by chemicals or bile duct ligation were also excluded.

2. Technical Overview of Genetic Mouse Models of BTC

There are several different platforms for genetic modeling of BTC in mice, generating considerable variations in the latency and penetrance of tumor development, cost, equipment, technique required for the models, and the experimental settings. Thus, thorough considerations are advisable before selecting the type of model to be generated. Several options can be selected for the genetic modeling of BTC in mice. These include the target cell type, the method used in genetic engineering, the type of host mouse, and the location of tumor development (Figure 2). In this section, we review the technical aspects of these options.
Cancers 13 02292 g002 550
Figure 2. Options in implantation-based modeling of BTC. (See Table 1 for the details of each study.) As examples of options for modeling BTC, target cell selection (A) and host selection (B) are illustrated. Abbreviations are: IHBD, intrahepatic bile duct and EHBD, extrahepatic bile duct. Nude mice and C57BL/6J strain mice were used as representatives for immunodeficient mice and immunocompetent mice, respectively.
Table 1. Implantation- and organoid-based hybrid model of biliary tract cancer in mice.

Driver

Oncogenes

Genotype of Organoids *

Methods for Genetic

Engineering **

Host

Implantation

Ref.
   

Oncogenes

TSGs

      

HCC (Hepatocellular Carcinoma) from Liver Organoid

cMyc

WT

cDNA (R)

shRNA (R); Trp53 and CRISPR/Cas9 (T); Apc

C57BL/6J

liver

[18]

iCCA (Intrahepatic Cholangiocelular Carcinoma) from Liver Organoid

KrasG12D

KrasLSL-G12D/+

Cre (L)

shRNA (L): Cdkn2a and/or Pten, Trp53, Apc

Nude

s.c.

[19]

KrasLSL-G12D/+; Trp53flox/flox

N.T.

Pik3caH1047R

Pik3caH1047R

shRNA (L): Cdkn2a, Pten,

Rosa26- Pik3caH1047R; Trp53flox/flox

N.T.

FGFR2-AHCYL1

WT

cDNA(R)

shRNA (L): Cdkn2a and/or Pten

KrasG12D

KrasLSL-G12D/+; Trp53flox/flox (outbred)

Cre (R)

N.T. or shRNA (R): Pten

NSG

s.c. or liver

[18]

KrasLSL-G12D/+

Cre (T)

CRISPR/Cas9 (T): Pten and Trp53

C57BL/6J

liver

FGFR2-BICC1, -MGEA5, -TACC3

Trp53−/−

cDNA (R)

N.T.

NOD-SCID

s.c. or liver

[20]

KRASG12V

Cdkn2a−/−

cDNA (R)

  

C57BL/6J

s.c., liver, or kidney

[21]

eCCA (Extrahepatic Cholangiocelular Carcinoma) from CBD Organoid

KrasG12D

KrasLSL-G12D; Tgfbr2flox/flox; Cdh1flox/flox

Cre (L)

N.T.

Nude or C57BL/6J

s.c.

[22]

KRASG12V

Cdkn2a−/−

cDNA (R)

N.T.

C57BL/6J

s.c., liver, or kidney

[21]

GBC (Gallbladder Carcinoma) from GB Organoid

KrasG12D

KrasLSL-G12D

Cre (L)

shRNA (L): Cdkn2a, Pten

Nude

s.c.

[19]

KrasLSL-G12D/+; Trp53flox/flox

N.T.

KRASG12V

Cdkn2a−/−

cDNA (R)

N.T.

C57BL/6J

s.c., liver, or kidney

[21]

KrasG12D

WT

Cre (T)

CRISPR/Cas9 (T): Pten and Trp53

C57BL/6J

s.c. or GB

[23]

ERBB2S310F or V777L

cDNA (R)

CRISPR/Cas9 (T): Trp53

NSG

s.c.
 

Rosa26- Pik3caH1047R; Trp53flox/flox

Cre (L)

N.T.

Nude

s.c.

[24]

KrasG12D

KrasLSL-G12D

CRISPR/Cas9 (T): Trp53, p19Arf, Smad4

C57BL/6J

GB via s.c.

For those models that developed cancer, pre-cancerous lesion and cystic lesions were listed. Note that liver organoid-derived tumor are either HCC or CCA (adenocarcinoma), but not mixed type liver cancer * C57BL/6J background unless otherwise indicated. ** L, lentivirus; R, retrovirus; T, transfection; N.T., not tested. Abbreviations: TSG, tumor suppressor genes; s.c., subcutis; WT, wildtype; CBD, common bile duct; GB, gallbladder.

3. In Vivo GEM Model of BTC

Owing to Alb expression in hepatoblasts, which are bi-potential progenitors for hepatocytes and cholangiocytes, liver-specific tumor models have been generated mostly by intercrossing Alb-Cre mice with conditional GEMs carrying floxed alleles. However, the histology of the resulting tumors varies among HCC, iCCA, and the mixed type, depending on the reconstitution of genetic alterations. For example, in mice with liver-specific homozygous deletion of Smad4 and Pten (hereafter Alb-Cre; Smad4f/f; Ptenf/f), all mice developed iCCA and died after 10 months, while Alb-Cre; Ptenf/f mice predominantly developed HCC [25]. In Alb-Cre; Ptenf/f; KrasLSL-G12D/+ mice, only iCCA was observed, while both iCCA and HCC were observed in Alb-Cre; Ptenf/+; KrasLSL-G12D/+ mice [26]. Considering that many factors can affect the development of iCCA and HCC, it is challenging to generate genuine iCCA or HCC separately by genetic aberrations in a deterministic way. Other mouse models for iCCA were mixed with HCC to varying extents, including Alb-Cre, KrasLSL-G12D/+, Trp53f/f, Alb-Cre, KrasLSL-G12D/+, Ptenf/f, Alb-Cre; KrasLSL-G12D/+; Idh1f/f, Alb-Cre; Notch1; KrasLSL-G12D/+, Alb-Cre; KrasLSL-G12D/+; Fbxw7f/f, and Alb-Cre; Cdh1f/f; Sav1f/f; Hspd1f/f [26][27][28][29][30][31][32][33][34].
Krt19-Cre is often used to induce genetic alterations in the biliary system, although Krt19 expression can also be detected in many glandular epithelia and non-keratinized squamous basal cells throughout the body [35]. In contrast, Krt19-Cre, KrasLSL-G12D/+, Tgfbr2f/f, and Cdh1f/f mice invariably developed eCCA and Krt19-Cre, KrasLSL-G12D/+, and Tgfbr2f/f mice died from respiratory cancers without eCCA development [22]. These results suggest that the lack of tissue specificity could impair the relevance of BTC models, especially when other organs become more cancer-prone. There are no known genes specifically expressed in GB. Nonetheless, Pdx1-Cre, often used to induce pancreatic carcinogenesis, also developed GBC by crossing with KrasLSL-G12D/+ mice [36]. Transgenic mice expressing rat ErbB-2 under the bovine keratin 5 promoter, which was aimed at developing skin tumors, also developed GBC [37][38], underscoring the oncogenic potential of ErbB-2.

4. Implantation-Based Hybrid Mouse Model of BTC

Although GEM is currently the gold standard in modeling tumorigenesis, it is still impossible to perfectly phenocopy all aspects of sporadic carcinogenesis. For example, currently available Cre mice may not provide sufficient tissue specificity, and the resultant gene recombination is homogenously observed across the target organ during development. In contrast, the tumor originates from a single mutated cell in adults, among many genetically intact normal cells in the organ. To address these issues, novel hybrid models have been developed by combining the in vitro genetic engineering of primary cells and subsequent implantation into host mice in various types of cancers, including BTC, intestine, lung, and pancreas [19][39][40][41][42][43]. This hybrid approach can also integrate GEM as a source of primary cells, thereby accelerating the modeling of BTC without multiple intercrossings to generate many GEMs. The implementation- and organoid-based BTC models are summarized in Table 1.

This entry is adapted from the peer-reviewed paper 10.3390/cancers13102292

References

  1. Banales, J.M.; Marin, J.J.G.; Lamarca, A.; Rodrigues, P.M.; Khan, S.A.; Roberts, L.R.; Cardinale, V.; Carpino, G.; Andersen, J.B.; Braconi, C.; et al. Cholangiocarcinoma 2020: The next horizon in mechanisms and management. Nat. Rev. Gastroenterol. Hepatol. 2020, 17, 557–588.
  2. Khan, S.A.; Tavolari, S.; Brandi, G. Cholangiocarcinoma: Epidemiology and risk factors. Liver Int. 2019, 39, 19–31.
  3. Bertuccio, P.; Malvezzi, M.; Carioli, G.; Hashim, D.; Boffetta, P.; El-Serag, H.B.; La Vecchia, C.; Negri, E. Global trends in mortality from intrahepatic and extrahepatic cholangiocarcinoma. J. Hepatol. 2019, 71, 104–114.
  4. Florio, A.A.; Ferlay, J.; Znaor, A.; Ruggieri, D.; Alvarez, C.S.; Laversanne, M.; Bray, F.; McGlynn, K.A.; Petrick, J.L. Global trends in intrahepatic and extrahepatic cholangiocarcinoma incidence from 1993 to 2012. Cancer 2020, 126, 2666–2678.
  5. Ainechi, S.; Lee, H. Updates on Precancerous Lesions of the Biliary Tract: Biliary Precancerous Lesion. Arch. Pathol. Lab. Med. 2016, 140, 1285–1289.
  6. Kendall, T.; Verheij, J.; Gaudio, E.; Evert, M.; Guido, M.; Goeppert, B.; Carpino, G. Anatomical, histomorphological and molecular classification of cholangiocarcinoma. Liver Int. 2019, 39, 7–18.
  7. Chan-On, W.; Nairismagi, M.L.; Ong, C.K.; Lim, W.K.; Dima, S.; Pairojkul, C.; Lim, K.H.; McPherson, J.R.; Cutcutache, I.; Heng, H.L.; et al. Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers. Nat. Genet. 2013, 45, 1474–1478.
  8. Jiao, Y.; Pawlik, T.M.; Anders, R.A.; Selaru, F.M.; Streppel, M.M.; Lucas, D.J.; Niknafs, N.; Guthrie, V.B.; Maitra, A.; Argani, P.; et al. Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas. Nat. Genet. 2013, 45, 1470–1473.
  9. Jusakul, A.; Cutcutache, I.; Yong, C.H.; Lim, J.Q.; Huang, M.N.; Padmanabhan, N.; Nellore, V.; Kongpetch, S.; Ng, A.W.T.; Ng, L.M.; et al. Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma. Cancer Discov. 2017, 7, 1116–1135.
  10. Li, M.; Zhang, Z.; Li, X.; Ye, J.; Wu, X.; Tan, Z.; Liu, C.; Shen, B.; Wang, X.A.; Wu, W.; et al. Whole-exome and targeted gene sequencing of gallbladder carcinoma identifies recurrent mutations in the ErbB pathway. Nat. Genet. 2014, 46, 872–876.
  11. Ong, C.K.; Subimerb, C.; Pairojkul, C.; Wongkham, S.; Cutcutache, I.; Yu, W.; McPherson, J.R.; Allen, G.E.; Ng, C.C.; Wong, B.H.; et al. Exome sequencing of liver fluke-associated cholangiocarcinoma. Nat. Genet. 2012, 44, 690–693.
  12. Sia, D.; Losic, B.; Moeini, A.; Cabellos, L.; Hao, K.; Revill, K.; Bonal, D.; Miltiadous, O.; Zhang, Z.; Hoshida, Y.; et al. Massive parallel sequencing uncovers actionable FGFR2-PPHLN1 fusion and ARAF mutations in intrahepatic cholangiocarcinoma. Nat. Commun. 2015, 6, 6087.
  13. Zou, S.; Li, J.; Zhou, H.; Frech, C.; Jiang, X.; Chu, J.S.; Zhao, X.; Li, Y.; Li, Q.; Wang, H.; et al. Mutational landscape of intrahepatic cholangiocarcinoma. Nat. Commun. 2014, 5, 5696.
  14. Nakamura, H.; Arai, Y.; Totoki, Y.; Shirota, T.; Elzawahry, A.; Kato, M.; Hama, N.; Hosoda, F.; Urushidate, T.; Ohashi, S.; et al. Genomic spectra of biliary tract cancer. Nat. Genet. 2015, 47, 1003–1010.
  15. Massa, A.; Varamo, C.; Vita, F.; Tavolari, S.; Peraldo-Neia, C.; Brandi, G.; Rizzo, A.; Cavalloni, G.; Aglietta, M. Evolution of the Experimental Models of Cholangiocarcinoma. Cancers 2020, 12, 2308.
  16. Leiting, J.L.; Murphy, S.J.; Bergquist, J.R.; Hernandez, M.C.; Ivanics, T.; Abdelrahman, A.M.; Yang, L.; Lynch, I.; Smadbeck, J.B.; Cleary, S.P.; et al. Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine. JHEP Rep. 2020, 2, 100068.
  17. Waddell, S.H.; Boulter, L. Developing models of cholangiocarcinoma to close the translational gap in cancer research. Expert Opin. Investig. Drugs 2021, 30, 439–450.
  18. Saborowski, A.; Wolff, K.; Spielberg, S.; Beer, B.; Hartleben, B.; Erlangga, Z.; Becker, D.; Dow, L.E.; Marhenke, S.; Woller, N.; et al. Murine Liver Organoids as a Genetically Flexible System to Study Liver Cancer In Vivo and In Vitro. Hepatol. Commun. 2019, 3, 423–436.
  19. Ochiai, M.; Yoshihara, Y.; Maru, Y.; Tetsuya, M.; Izumiya, M.; Imai, T.; Hippo, Y. Kras-driven heterotopic tumor development from hepatobiliary organoids. Carcinogenesis 2019, 40, 1142–1152.
  20. Cristinziano, G.; Porru, M.; Lamberti, D.; Buglioni, S.; Rollo, F.; Amoreo, C.A.; Manni, I.; Giannarelli, D.; Cristofoletti, C.; Russo, G.; et al. FGFR2 fusion proteins drive oncogenic transformation of mouse liver organoids towards cholangiocarcinoma. J. Hepatol. 2021.
  21. Kasuga, A.; Semba, T.; Sato, R.; Nobusue, H.; Sugihara, E.; Takaishi, H.; Kanai, T.; Saya, H.; Arima, Y. Oncogenic KRAS-expressing organoids with biliary epithelial stem cell properties give rise to biliary tract cancer in mice. Cancer Sci. 2021, 112, 1822–1838.
  22. Nakagawa, H.; Suzuki, N.; Hirata, Y.; Hikiba, Y.; Hayakawa, Y.; Kinoshita, H.; Ihara, S.; Uchino, K.; Nishikawa, Y.; Ijichi, H.; et al. Biliary epithelial injury-induced regenerative response by IL-33 promotes cholangiocarcinogenesis from peribiliary glands. Proc. Natl. Acad. Sci. USA 2017, 114, E3806–E3815.
  23. Erlangga, Z.; Wolff, K.; Poth, T.; Peltzer, A.; Nahnsen, S.; Spielberg, S.; Timrott, K.; Woller, N.; Kuhnel, F.; Manns, M.P.; et al. Potent Antitumor Activity of Liposomal Irinotecan in an Organoid- and CRISPR-Cas9-Based Murine Model of Gallbladder Cancer. Cancers 2019, 11, 1904.
  24. Kato, S.; Fushimi, K.; Yabuki, Y.; Maru, Y.; Hasegawa, S.; Matsuura, T.; Kurotaki, D.; Suzuki, A.; Kobayashi, N.; Yoneda, M.; et al. Precision modeling of gall bladder cancer patients in mice based on orthotopic implantation of organoid-derived tumor buds. Oncogenesis 2021, 10, 33.
  25. Xu, X.; Kobayashi, S.; Qiao, W.; Li, C.; Xiao, C.; Radaeva, S.; Stiles, B.; Wang, R.H.; Ohara, N.; Yoshino, T.; et al. Induction of intrahepatic cholangiocellular carcinoma by liver-specific disruption of Smad4 and Pten in mice. J. Clin. Investig. 2006, 116, 1843–1852.
  26. Ikenoue, T.; Terakado, Y.; Nakagawa, H.; Hikiba, Y.; Fujii, T.; Matsubara, D.; Noguchi, R.; Zhu, C.; Yamamoto, K.; Kudo, Y.; et al. A novel mouse model of intrahepatic cholangiocarcinoma induced by liver-specific Kras activation and Pten deletion. Sci. Rep. 2016, 6, 23899.
  27. Galicia, V.A.; He, L.; Dang, H.; Kanel, G.; Vendryes, C.; French, B.A.; Zeng, N.; Bayan, J.A.; Ding, W.; Wang, K.S.; et al. Expansion of hepatic tumor progenitor cells in Pten-null mice requires liver injury and is reversed by loss of AKT2. Gastroenterology 2010, 139, 2170–2182.
  28. Hill, M.A.; Alexander, W.B.; Guo, B.; Kato, Y.; Patra, K.; O’Dell, M.R.; McCall, M.N.; Whitney-Miller, C.L.; Bardeesy, N.; Hezel, A.F. Kras and Tp53 Mutations Cause Cholangiocyte- and Hepatocyte-Derived Cholangiocarcinoma. Cancer Res. 2018, 78, 4445–4451.
  29. Ikenoue, T.; Terakado, Y.; Zhu, C.; Liu, X.; Ohsugi, T.; Matsubara, D.; Fujii, T.; Kakuta, S.; Kubo, S.; Shibata, T.; et al. Establishment and analysis of a novel mouse line carrying a conditional knockin allele of a cancer-specific FBXW7 mutation. Sci. Rep. 2018, 8, 2021.
  30. Lee, K.P.; Lee, J.H.; Kim, T.S.; Kim, T.H.; Park, H.D.; Byun, J.S.; Kim, M.C.; Jeong, W.I.; Calvisi, D.F.; Kim, J.M.; et al. The Hippo-Salvador pathway restrains hepatic oval cell proliferation, liver size, and liver tumorigenesis. Proc. Natl. Acad. Sci. USA 2010, 107, 8248–8253.
  31. Lin, Y.K.; Fang, Z.; Jiang, T.Y.; Wan, Z.H.; Pan, Y.F.; Ma, Y.H.; Shi, Y.Y.; Tan, Y.X.; Dong, L.W.; Zhang, Y.J.; et al. Combination of Kras activation and PTEN deletion contributes to murine hepatopancreatic ductal malignancy. Cancer Lett. 2018, 421, 161–169.
  32. O’Dell, M.R.; Huang, J.L.; Whitney-Miller, C.L.; Deshpande, V.; Rothberg, P.; Grose, V.; Rossi, R.M.; Zhu, A.X.; Land, H.; Bardeesy, N.; et al. Kras(G12D) and p53 mutation cause primary intrahepatic cholangiocarcinoma. Cancer Res. 2012, 72, 1557–1567.
  33. Saha, S.K.; Parachoniak, C.A.; Ghanta, K.S.; Fitamant, J.; Ross, K.N.; Najem, M.S.; Gurumurthy, S.; Akbay, E.A.; Sia, D.; Cornella, H.; et al. Mutant IDH inhibits HNF-4alpha to block hepatocyte differentiation and promote biliary cancer. Nature 2014, 513, 110–114.
  34. Zender, S.; Nickeleit, I.; Wuestefeld, T.; Sorensen, I.; Dauch, D.; Bozko, P.; El-Khatib, M.; Geffers, R.; Bektas, H.; Manns, M.P.; et al. A critical role for notch signaling in the formation of cholangiocellular carcinomas. Cancer Cell 2013, 23, 784–795.
  35. Means, A.L.; Xu, Y.; Zhao, A.; Ray, K.C.; Gu, G. A CK19(CreERT) knockin mouse line allows for conditional DNA recombination in epithelial cells in multiple endodermal organs. Genesis 2008, 46, 318–323.
  36. Chung, W.C.; Wang, J.; Zhou, Y.; Xu, K. Kras(G12D) upregulates Notch signaling to induce gallbladder tumorigenesis in mice. Oncoscience 2017, 4, 131–138.
  37. Kiguchi, K.; Bol, D.; Carbajal, S.; Beltran, L.; Moats, S.; Chan, K.; Jorcano, J.; DiGiovanni, J. Constitutive expression of erbB2 in epidermis of transgenic mice results in epidermal hyperproliferation and spontaneous skin tumor development. Oncogene 2000, 19, 4243–4254.
  38. Kiguchi, K.; Carbajal, S.; Chan, K.; Beltran, L.; Ruffino, L.; Shen, J.; Matsumoto, T.; Yoshimi, N.; DiGiovanni, J. Constitutive expression of ErbB-2 in gallbladder epithelium results in development of adenocarcinoma. Cancer Res. 2001, 61, 6971–6976.
  39. Onuma, K.; Ochiai, M.; Orihashi, K.; Takahashi, M.; Imai, T.; Nakagama, H.; Hippo, Y. Genetic reconstitution of tumorigenesis in primary intestinal cells. Proc. Natl. Acad. Sci. USA 2013, 110, 11127–11132.
  40. Maru, Y.; Onuma, K.; Ochiai, M.; Imai, T.; Hippo, Y. Shortcuts to intestinal carcinogenesis by genetic engineering in organoids. Cancer Sci. 2019, 110, 858–866.
  41. Matsuura, T.; Maru, Y.; Izumiya, M.; Hoshi, D.; Kato, S.; Ochiai, M.; Hori, M.; Yamamoto, S.; Tatsuno, K.; Imai, T.; et al. Organoid-based ex vivo reconstitution of Kras-driven pancreatic ductal carcinogenesis. Carcinogenesis 2020, 41, 490–501.
  42. Sato, T.; Morita, M.; Tanaka, R.; Inoue, Y.; Nomura, M.; Sakamoto, Y.; Miura, K.; Ito, S.; Sato, I.; Tanaka, N.; et al. Ex vivo model of non-small cell lung cancer using mouse lung epithelial cells. Oncol. Lett. 2017, 14, 6863–6868.
  43. Naruse, M.; Masui, R.; Ochiai, M.; Maru, Y.; Hippo, Y.; Imai, T. An organoid-based carcinogenesis model induced by in vitro chemical treatment. Carcinogenesis 2020, 41, 1444–1453.
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