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首页> 外文期刊>European journal of cancer prevention: The official journal of the European Cancer Prevention Organisation (ECP) >Expression of KLF6-SV2 in colorectal cancer and its impact on proliferation and apoptosis
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Expression of KLF6-SV2 in colorectal cancer and its impact on proliferation and apoptosis

机译:KLF6-SV2在结直肠癌中的表达及其对增殖和凋亡的影响

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摘要

Kruppel like factor 6 (KLF6), a member of KLF family, which has classic zinc finger structure, is broadly considered to have anticancer activity. The role of SV2 variant, one of KLF6 alternative splicing isoforms has not yet been definite in the colorectal cancer. This study aimed to detect the expression of the KLF6-SV2 in colorectal cancer and investigate its impact on cell proliferation and apoptosis. qRT-PCR was used to quantitatively determine KLF6-SV2 mRNA expression in colorectal cancer samples, corresponding normal tissue, normal colonic mucosal cell line FHC and seven colorectal cancer cell lines. SW480 and SW620 cell models with over-expressing KLF6-SV2 were constructed. Cell proliferation, cell cycle and apoptosis were measured respectively using MTT assay, DNA ploidy detection and Annexin V flow cytometry. Meanwhile, expression of p53, p21 and Bax were detected by qRT-PCR and western blot. The mRNA expression level of KLF6-SV2 in colorectal cancer tissues (0.783 +/- 0.409) was decreased than in corresponding normal tissues (1.086 +/- 0.449) (P<0.01), and expression in SW480 and SW620 were lower than in FHC, HCT116, LoVo, HT29, Caco-2 and RKO. In cell lines over-expressing KLF6-SV2, cell proliferation was markedly suppressed, cell cycle was blocked and cell apoptosis was significantly induced. Simultaneously, expression of p21 and Bax were remarkably up-regulated, while p53 remained unchanged. Decreased expression of KLF6-SV2 may be associated with the occurrence and development of colorectal cancer. KLF6-SV2 plays a role as tumor suppressor by efficiently blocking cell proliferation, arresting cell cycle and inducing apoptosis in colorectal cancer, which may be related to increased expression of p21 and Bax.
机译:KRUPPEL类似因素6(KLF6),KLF系列具有经典锌手指结构的百姓,广泛地认为具有抗癌活动。 SV2变体的作用,KLF6替代剪接同种型之一尚未在结肠直肠癌中尚未确定。本研究旨在检测结直肠癌KLF6-SV2的表达,并研究其对细胞增殖和细胞凋亡的影响。 QRT-PCR用于定量确定结肠直肠癌样品中的KLF6-SV2 mRNA表达,相应的正常组织,正常结肠粘膜细胞系FHC和七种结肠癌细胞系。 SW480和SW620细胞模型具有过于表达的KLF6-SV2。分别使用MTT测定,DNA倍倍性检测和膜蛋白V流式细胞术分别测量细胞增殖,细胞周期和细胞凋亡。同时,通过QRT-PCR和Western印迹检测P53,P21和BAX的表达。直肠癌组织中KLF6-SV2的mRNA表达水平低于相应的正常组织(1.086 +/- 0.449)(P <0.01),SW480和SW620中的表达低于FHC ,hct116,lovo,ht29,caco-2和rko。在细胞系上过度表达的KLF6-SV2,细胞增殖被显着抑制,细胞周期被阻断,并且显着诱导细胞凋亡。同时,P21和Bax的表达显着上调,而P53保持不变。 KLF6-SV2的表达降低可能与结直肠癌的发生和发展有关。 KLF6-SV2通过有效地阻断细胞增殖,诱导结直肠癌中的细胞凋亡,诱导细胞增殖和诱导细胞凋亡,klf6-sv2发挥作用。

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