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NTRK3 Is a Potential Tumor Suppressor Gene Commonly Inactivated by Epigenetic Mechanisms in Colorectal Cancer

机译:NTRK3是一种潜在的肿瘤抑制基因通常在大肠癌中被表观遗传机制所灭活。

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摘要

NTRK3 is a member of the neurotrophin receptor family and regulates cell survival. It appears to be a dependence receptor, and thus has the potential to act as an oncogene or as a tumor suppressor gene. NTRK3 is a receptor for NT-3 and when bound to NT-3 it induces cell survival, but when NT-3 free, it induces apoptosis. We identified aberrantly methylated NTRK3 in colorectal cancers through a genome-wide screen for hypermethylated genes. This discovery led us to assess whether NTRK3 could be a tumor suppressor gene in the colon. NTRK3 is methylated in 60% of colon adenomas and 67% of colon adenocarcinomas. NTRK3 methylation suppresses NTRK3 expression. Reconstitution of NTRK3 induces apoptosis in colorectal cancers, if NT-3 is absent. Furthermore, the loss of NTRK3 expression associates with neoplastic transformation in vitro and in vivo. We also found that a naturally occurring mutant NTRK3 found in human colorectal cancer inhibits the tumor suppressor activity of NTRK3. In summary, our findings suggest NTRK3 is a conditional tumor suppressor gene that is commonly inactivated in colorectal cancer by both epigenetic and genetic mechanisms whose function in the pathogenesis of colorectal cancer depends on the expression status of its ligand, NT-3.
机译:NTRK3是神经营养蛋白受体家族的成员,并调节细胞存活。它似乎是依赖性受体,因此有潜力充当癌基因或抑癌基因。 NTRK3是NT-3的受体,当与NT-3结合时,它诱导细胞存活,但是当不含NT-3时,它诱导细胞凋亡。我们通过全甲基化的全基因组筛查在大肠癌中发现了异常甲基化的NTRK3。这一发现使我们评估了NTRK3是否可能是结肠中的抑癌基因。 NTRK3在60%的结肠腺瘤和67%的结肠腺癌中被甲基化。 NTRK3甲基化抑制NTRK3表达。如果不存在NT-3,则NTRK3的重组会诱导大肠癌的凋亡。此外,在体外和体内,NTRK3表达的丧失与肿瘤转化有关。我们还发现在人类大肠癌中发现的天然突变体NTRK3抑制了NTRK3的抑癌活性。总而言之,我们的发现表明NTRK3是一种条件性肿瘤抑制基因,在结直肠癌中通常通过表观遗传和遗传机制使其失活,其在结直肠癌发病机理中的功能取决于其配体NT-3的表达状态。

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