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Sox2 在人宫颈癌发生中的表达。

Expression of Sox2 in human cervical carcinogenesis.

机构信息

Department of Reproductive Medicine, the First Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, The People's Republic of China.

出版信息

Hum Pathol. 2010 Oct;41(10):1438-47. doi: 10.1016/j.humpath.2009.11.021. Epub 2010 Aug 14.

Abstract

Sox2 is a key transcription factor for embryonic development and plays a critical role in determining the fate of stem cells. Recently, Sox2 has been detected in several human tumors, indicating a potential function in tumorigenesis. We initially reported remarkably increased nuclear Sox2 staining in cervical carcinomas compared with normal cervix (P < .05). Furthermore, Sox2 staining was detected in most tumorsphere cells isolated from fresh cervical cancer tissues but not among the differentiated tumorsphere cells. When Sox2 was stably expressed in cervical cancer cells (SiHa and HeLa), Sox2-overexpressing cells had increased proliferation, clonogenicity, and tumorigenicity in vitro and in vivo than control cells. These results suggest that Sox2 may participate in carcinogenesis of cervical carcinomas and may be a potential therapeutic target molecule for cervical cancers.

摘要

Sox2 是胚胎发育的关键转录因子,在决定干细胞命运方面发挥着关键作用。最近,Sox2 在几种人类肿瘤中被检测到,表明其在肿瘤发生中可能具有功能。我们最初报道,与正常宫颈相比,宫颈癌中 Sox2 的核染色显著增加(P<0.05)。此外,从新鲜宫颈癌组织中分离的肿瘤球细胞中检测到 Sox2 染色,但在分化的肿瘤球细胞中未检测到。当 Sox2 在宫颈癌细胞(SiHa 和 HeLa)中稳定表达时,与对照细胞相比,Sox2 过表达细胞在体外和体内具有更高的增殖、集落形成和致瘤性。这些结果表明,Sox2 可能参与宫颈癌的癌变过程,可能是宫颈癌的潜在治疗靶点分子。

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