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Rocchetti, M.T.; Bellanti, F.; Fiocco, D.; Mangieri, D. Luteolin. Encyclopedia. Available online: https://encyclopedia.pub/entry/45036 (accessed on 25 December 2024).
Rocchetti MT, Bellanti F, Fiocco D, Mangieri D. Luteolin. Encyclopedia. Available at: https://encyclopedia.pub/entry/45036. Accessed December 25, 2024.
Rocchetti, Maria Teresa, Francesco Bellanti, Daniela Fiocco, Domenica Mangieri. "Luteolin" Encyclopedia, https://encyclopedia.pub/entry/45036 (accessed December 25, 2024).
Rocchetti, M.T., Bellanti, F., Fiocco, D., & Mangieri, D. (2023, May 31). Luteolin. In Encyclopedia. https://encyclopedia.pub/entry/45036
Rocchetti, Maria Teresa, et al. "Luteolin." Encyclopedia. Web. 31 May, 2023.
Luteolin
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This entry is adapted from the peer-reviewed paper 10.3390/ijms24108824

Luteolin (3′,4′,5,7-tetrahydroxyflavone), a member of the flavonoid family derived from plants and fruits, shows a wide range of biomedical applications. In fact, due to its anti-inflammatory, antioxidant and immunomodulatory activities, Asian medicine has been using luteolin for centuries to treat several human diseases, including arthritis, rheumatism, hypertension, neurodegenerative disorders and various infections. Of note, luteolin displays many anti-cancer/anti-metastatic properties.

phytochemicals flavonoids metastasis prevention signaling pathways

1. Luteolin

Luteolin is a flavonoid belonging to the flavone family; it is isolated from several vegetables and edible herbs, including radicchio, broccoli, raw brussels sprouts, onion leaves, parsley, carrots, peppers and rosemary, where it can occur either as aglycone or bound to one or several carbohydrates as glycoside [1] (Figure 1).
Ijms 24 08824 g002 550
Figure 1. Main sources of luteolin. Edible vegetables, such as radicchio, broccoli, raw brussels sprouts, onion leaves, parsley, carrots, peppers and rosemary are rich in luteolin.
Luteolin is extracted as a yellow crystalline compound and its chemical structure presents a classic flavone C6-C3-C6 skeleton, consisting in two benzene rings with 4 hydroxyl groups located at positions 3, 4, 5 and 7, and one oxygen-containing ring which presents a C2-C3 double bond [1]. All these functional groups account for the biological/biochemical properties of luteolin, some of them being specifically involved in maintaining redox balance in various pathological processes [2][3] (Figure 2).
Ijms 24 08824 g003 550
Figure 2. Chemical structure of luteolin (3,4,5,7-tetrahydroxy flavone). Luteolin is a flavone belonging to a group of hydrophobic, naturally occurring compounds, named flavonoids. The functional groups involved in oxido-reductive properties are marked in red.
In fact, preclinical studies ascribed to luteolin several pharmacological properties, including anti-inflammatory, neuroprotective, antimicrobial/antiviral, cardioprotective, antidiabetic and pro-/antioxidant effects [4]. Interestingly, since this flavone can interact with various signaling pathways, experimental evidence attributes to luteolin important chemopreventive effects, indicating its ability to interfere with almost all cellular processes underlying cancer development, including metastasis formation [5][6][7]. The available data related to the pharmacokinetics of the free or glycosylated forms of luteolin derive mainly from studies on rat models [8][9][10]. Despite the numerous beneficial effects already mentioned, studies on absorption, metabolism and bioavailability of luteolin in humans are very difficult, partly due to its hydrophobicity, which affects bioavailability and limits the yields of the bioactive flavonoid [4].

2. Luteolin Affects the Epithelial-Mesenchymal Transition

EMT is the differentiation process of epithelial cells toward mesenchymal ones; several events are observed during this process, including a disorganization of epithelial cell polarity, the dissolution of cellular junctions, as well as a reorganization of the cytoskeleton [11][12][13]. Thus, EMT involves the downregulation of epithelial markers expression, such as E-cadherin, claudins, zonula occludens-1 (ZO-1), and the acquisition of many facets of the mesenchymal cells, including the expression of N-cadherin and vimentin, coupled with a high propensity to cell motility, invasiveness, and resistance to anoikis [12][13][14]. Several signaling pathways have been identified in EMT induction, such as the transforming growth factor-beta (TGF-β), Notch, Wnt/β-catenin, as well as the Hippo-YAP/TAZ pathways [15][16]. Moreover, several transcription factors (and their target genes) promote EMT, including Snail1/2, Twist1/2, ZEB1/2 and hypoxia-inducible factors 1/2 (HIF1/2) [17]. Physiologically, EMT occurs during embryonic development and in tissue remodeling. In cancer, this process assumes a crucial role in promoting metastasis [12][13]. Therefore, blocking or reversing EMT may represent an attractive approach to prevent cancer spreading [13].
As aforementioned, luteolin inhibits or prevents cell invasion and metastasis in several cancer types, due to a modulation of EMT [18]. In this regard, both in vitro and in vivo studies demonstrated that treatment of highly metastatic triple-negative breast cancer (TNBC) with luteolin reduced β-catenin expression and downregulated mesenchymal markers, such as N-cadherin, vimentin, Snail and Slug [19]. Moreover, cancer cells regained their epithelial features by overexpressing cell-cell junctional proteins, such as E-cadherin and claudins [19].
MicroRNAs (miRs) are small, endogenous, noncoding RNAs that can post-transcriptionally regulate gene expression and play an important role in maintaining normal cellular functions [20]. On the other hand, growing evidence shows that some miRs participate in the initiation and progression of cancer, taking part in the EMT process [21][22]. Luteolin was able to reverse EMT in breast cancer cells (MDA-MB-453 and MCF-7) by overexpressing miR-230, which, in turn, inhibited the Ras/Raf/MEK/ERK signaling pathway, known as a marker of cancer invasiveness [23]. Furthermore, luteolin administration significantly inhibited gastric carcinoma (GC) upregulating miR-139, miR-34a, miR-422a, miR-107 levels, while suppressing the oncogenic expression of miR-21, miR-155, miR-224, miR-340 [24]. Regulation of this panel of miRs was accompanied by reduced cell proliferation, cell cycle arrest, and induction of apoptosis [24]. In a different study, the flavonoid inhibited the oncogenic properties of YAP/TAZ in highly metastatic breast cancer, both in vitro and in xenograft models [25]. Moreover, Zang et al. demonstrated that, by interfering with Notch1 and Akt/β-catenin signaling in GC, luteolin reversed the EMT process and, consequently, inhibited tumor progression and invasion, both in vitro and in vivo [26]. By using cultures of human lung adenocarcinoma cells (A549), Chen et al. showed that luteolin inhibited cell proliferation and migration through an attenuation of TGF-β1-induced EMT, by activating the PI3K/Akt–NF-κB–Snail signaling pathway [27]. Furthermore, luteolin (in a time- and dose-dependent manner) reversed IL-6-induced EMT acting on STAT3 signaling and, consequently, reduced the invasiveness of cancer cells by inhibiting the release of metalloproteases (MMPs) in in vitro models of human pancreatic cancer (i.e., Panc-1 and SW1990 cells) [28].
As abovementioned, HIF-1 and HIF-2 are implicated in cancer-associated EMT [17]. Based on these premises, Li et al. observed that luteolin, by inhibiting the HIF-1α/VEGF signaling pathway, decreased the expression of N-cadherin and vimentin mesenchymal markers, while augmenting the level of epithelial cadherin isoform in human and murine melanoma cells (i.e., A375 and B16-F10 cell lines, respectively) [29]. The inversion of hypoxia-induced EMT was also observed in a murine melanoma model, where luteolin inhibited lung metastasis formation by stopping the β3 integrin/FAK signaling pathway [30]. Similarly, luteolin prevented hypoxia-induced EMT of human non-small cell lung carcinoma cells (NSCLC; A549 and NCI-H1975 cell lines), as evidenced by a downregulation of mesenchymal specific markers, such as vimentin and N-cadherin; contextually, luteolin treatment repressed cancer cell motility and adhesion, interfering with integrin β1 expression and with the FAK-signaling pathway [31].
The ability of luteolin to reverse EMT in cancer cells is often enhanced by adding other flavonoids, such as quercetin [32][33]. Indeed, a mixture of luteolin and quercetin was able to attenuate (in a time- and dose-dependent manner) EMT-correlated events, migration and invasiveness of human squamous carcinoma, both in vivo and in vitro, by suppressing the Src/Stat3/S100A signaling pathway [32]. Similarly, the addition of luteolin to quercetin inhibited metastasis of skin squamous carcinoma by blocking the Akt/mTOR/c-Myc signaling pathway to suppress RPS19-activated EMT signaling [33].
In summary, luteolin appears capable to block or reverse EMT by acting on multiple molecular targets, hindering the first steps of cancer spreading (Figure 3).
Ijms 24 08824 g004 550
Figure 3. Luteolin interferes with the epithelial-mesenchymal transition. The flavone inhibits or reverses EMT. TJs: Tights Junctions; AJs; Adherens Junctions.

3. Luteolin Suppresses Angiogenesis

Angiogenesis is the process by which new blood vessels form, starting from preexisting vasculature; this event depends on pro-angiogenic mediators, such as vascular endothelial growth factor (VEGF), basic-fibroblast growth factor (bFGF), metalloproteases, etc., and on negative regulators of angiogenesis, including thrombospondin and endostatin [34]. Angiogenesis plays a crucial role during a variety of physiological processes, such as wound healing, embryonic development and pregnancy [34]. On the other hand, neovascularization is a key event for pathological processes, such as tumor progression, invasion and metastatic cascade [35]. This last aspect is pharmacologically relevant: in fact, many authorized cancer therapies are directed against the tumor-associated vessels [35][36][37][38].
Several investigations demonstrate that various flavonoids—including luteolin—act as negative regulators of VEGF and other pro-angiogenic factors [39][40][41]. For instance, Cai and co-workers demonstrated that luteolin decreased VEGF secretion and VEGF mRNA expression in pancreatic carcinoma cells (PANC-1, CoLo-357 and BxPC-3 cell lines), via inhibition of the NF-κB transcriptional factor activity [42]. Furthermore, treating human choroidal melanoma cells (C918 and OCM-1) with luteolin not only inhibited VEGF expression, but also increased cancer cell death [43]. Additionally, an in vitro study on breast cancer showed that luteolin, by interfering with Notch1 expression, inhibited VEGF secretion from tumor cells, decreased endothelial cell migration, proliferation, and their propension to form tube-like structures on a Matrigel layer [44]. Cook and co-coworkers demonstrated the ability of luteolin to block the production of VEGF in human breast cancer cells (T47-D and BT-474) responsive to (natural and synthetic) progestins, both in vitro and in a xenograft model [45]. In a similar study, the authors showed that luteolin (in a dose- and time-dependent fashion) significantly reduced VEGF secretion in human TNBC cells (i.e., MDA- MB-435 and highly aggressive MDA-MB-231 (4175) LM2), coupled with a significantly decreased cell viability and reduced migration and invasion in vitro; at the same time, the authors showed that the flavonoid inhibited lung metastasis formation in a dedicated xenograft model [46].
The anti-proliferative/anti-mitotic effect on endothelial cells was also tested in infantile haemangioma in vitro and in vivo, by using haemangioma-derived stem cells (HemSC) [47]. In detail, the results demonstrated that luteolin suppressed VEGF expression and inhibited HemSC growth in a dose-dependent manner, and, at the same time, the flavonoid inhibited both angiogenesis and vasculogenesis, in a murine model, by acting on the frizzled6 (FZD6) signaling pathway [47]. In prostate cancer, luteolin strongly suppressed neovascularization in different experimental settings by inhibiting the activation of VEGFR-2/AKT/ERK/mTOR/P70S6K signaling pathways [48]. In fact, it abolished angiogenesis in an ex vivo chicken chorioallantoic membrane (CAM) assay and in a Matrigel plug assay; in addition, the flavone suppressed both vascularization and growth of the tumor in a xenograft model [48]. Moreover, luteolin inhibited different pathways of vascularization in an in vitro model of uveal melanoma, including angiogenesis, vasculogenesis and vasculogenic mimicry, by suppressing the PI3K/AKT signaling pathway [49].
As previously cited, miRs have a role in cancer evolution, including angiogenesis [22]. In an experimental model of NSCLC, luteolin repressed the expression of the rich element binding protein B (PURB) and crucial proangiogenic factors, including VEGF and MMP-2/-9, by overexpressing the miR-133a-p69 and by regulating MAPK and PI3K/Akt signaling pathways [50]. In breast cancer, the flavonoid upregulated the biogenesis of miR-34a, miR-181a, miR-139-5p, miR-224 and miR-246, while it decreased the level of miR-155, coupled with a significant inhibition of VEGF/Notch signaling and MMPs downregulation [51].
Tumor growth and its progression also depend on proangiogenic factors secreted by the surrounding microenvironment cells (e.g., fibroblasts, tumor associated macrophages (TAMs), etc.) [52]. Fang et al. demonstrated that luteolin inhibited the ability of TAMs to induce angiogenesis, thereby inhibiting tumor growth and its spreading, in both normoxic and hypoxic conditions [53].
Taken together, these studies show promise for luteolin as a potent anti-angiogenic agent, evading tumor evolution and metastatic cascade (Figure 4).
Ijms 24 08824 g005 550
Figure 4. Luteolin blocks neovascularization. The flavonoid blocks angiogenesis by negative regulation of pro-angiogenic mediators.

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Subjects: Oncology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Maria Teresa Rocchetti
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Francesco Bellanti
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Daniela Fiocco
,
Domenica Mangieri
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Update Date: 01 Jun 2023
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