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m A 去甲基化酶 ALKBH5 的抑制作用促进食管鳞状细胞癌的进展。

mA demethylase ALKBH5 suppression contributes to esophageal squamous cell carcinoma progression.

机构信息

Laboratory Animal Center, Southern Medical University, Guangzhou 510515, China.

Guangzhou Southern Medical Laboratory Animal Sci. & Tech. Co., Ltd., Guangzhou 510515, China.

出版信息

Aging (Albany NY). 2021 Sep 7;13(17):21497-21512. doi: 10.18632/aging.203490.

Abstract

Esophageal squamous cell carcinoma (ESCC) is a highly malignant gastrointestinal cancer with a high recurrence rate and poor prognosis. Although N-methyladenosine (mA), the most abundant epitranscriptomic modification of mRNAs, has been implicated in several cancers, little is known about its participation in ESCC progression. We found reduced expression of ALKBH5, an mA demethylase, in ESCC tissue specimens with a more pronounced effect in T3-T4, N1-N3, clinical stages III-IV, and histological grade III tumors, suggesting its involvement in advanced stages of ESCC. Exogenous expression of ALKBH5 inhibited the proliferation of ESCC cells, whereas depletion of endogenous ALKBH5 markedly enhanced ESCC cell proliferation . This suggests ALKBH5 exerts anti-proliferative effects on ESCC growth. Furthermore, ALKBH5 overexpression suppressed tumor growth of Eca-109 cells in nude mice; conversely, depletion of endogenous ALKBH5 accelerated tumor growth of TE-13 cells . The growth-inhibitory effects of ALKBH5 overexpression are partly attributed to a G1-phase arrest. In addition, ALKBH5 overexpression reduced the migration and invasion of ESCC cells. Altogether, our findings demonstrate that the loss of ALKBH5 expression contributes to ESCC malignancy.

摘要

食管鳞状细胞癌(ESCC)是一种高度恶性的胃肠道癌症,具有较高的复发率和较差的预后。尽管 N6-甲基腺苷(m6A)是 mRNA 中最丰富的转录后修饰之一,但其在 ESCC 进展中的作用仍知之甚少。我们发现 ALKBH5(一种 mA 去甲基化酶)在 ESCC 组织标本中的表达降低,在 T3-T4、N1-N3、临床分期 III-IV 和组织学分级 III 的肿瘤中表达降低更为明显,表明其参与了 ESCC 的晚期进展。ALKBH5 的外源性表达抑制了 ESCC 细胞的增殖,而内源性 ALKBH5 的耗竭则显著增强了 ESCC 细胞的增殖。这表明 ALKBH5 对 ESCC 生长具有抗增殖作用。此外,ALKBH5 的过表达抑制了裸鼠中 Eca-109 细胞的肿瘤生长;相反,内源性 ALKBH5 的耗竭加速了 TE-13 细胞的肿瘤生长。ALKBH5 过表达的生长抑制作用部分归因于 G1 期阻滞。此外,ALKBH5 的过表达降低了 ESCC 细胞的迁移和侵袭。总之,我们的研究结果表明,ALKBH5 表达的缺失导致了 ESCC 的恶性转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afcb/8457604/b8a4d2693691/aging-13-203490-g001.jpg

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