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TGF-β1 、TβR Ⅱ及cyclinD1 在大肠癌的表达及其意义[J]. 肿瘤防治研究, 2005, 32(01): 33-34. DOI: 10.3971/j.issn.1000-8578.1400
引用本文: TGF-β1 、TβR Ⅱ及cyclinD1 在大肠癌的表达及其意义[J]. 肿瘤防治研究, 2005, 32(01): 33-34. DOI: 10.3971/j.issn.1000-8578.1400
Signif icance of TGF-β1, TβRⅡand cyclinD1 Expression in Colorectal Carcinoma[J]. Cancer Research on Prevention and Treatment, 2005, 32(01): 33-34. DOI: 10.3971/j.issn.1000-8578.1400
Citation: Signif icance of TGF-β1, TβRⅡand cyclinD1 Expression in Colorectal Carcinoma[J]. Cancer Research on Prevention and Treatment, 2005, 32(01): 33-34. DOI: 10.3971/j.issn.1000-8578.1400

TGF-β1 、TβR Ⅱ及cyclinD1 在大肠癌的表达及其意义

Signif icance of TGF-β1, TβRⅡand cyclinD1 Expression in Colorectal Carcinoma

  • 摘要: 目的 探讨TGF-β1 、TβR Ⅱ及cyclinD1 在大肠癌发生发展过程中的作用。方法 采用免疫组化SP 法从蛋白水平分析TGF-β1 、TβR Ⅱ、cyclinD1 在大肠腺瘤及大肠癌组织中的表达情况。结果 TGF-β1 蛋白阳性表达率在腺瘤组织为28. 6 %, 大肠癌组织中为57. 1 %( P < 0. 05) ; TβR Ⅱ在大肠癌组织中的表达率为51. 8 %, 低于腺瘤组织( P < 0. 01) ; TGF-β1 、TβR Ⅱ表达的改变与大肠癌浸润深度、淋巴结转移有关; TβR Ⅱ和cyclinD1 的表达呈负相关( P < 0. 05) 。结论 TGF-β1 的过表达与大肠癌侵袭转移演进密切相关; TβR Ⅱ的失表达不仅有助于提高细胞对TGF-β1 的生长抵抗,也增强了大肠癌的侵袭性;cyclinD1 在TGF-β1 的生长抵抗中可能发挥了某些作用。

     

    Abstract: Objective  To investigate the role of TGF-β1, TβR Ⅱ,cyclinD1 expression in colorectal carcinoma. Methods  SP immunostaining technique was used to examine the expression of TGF-β1, TβR Ⅱand cyclinD1 in colorectal adenomas and carcinomas. Results  TGF-β1 was expressed positively in 28. 6 %colorectal adenoma tissues while 57. 1 % in carcinoma ( P < 0. 05 ) ; TβR Ⅱ was expressed positively 51. 8 % in colorectal carcinoma tissues which was lower than adenoma tissues ( P < 0. 01) ; The expression of TGF-β1 、TβR Ⅱin colorectal tissues was associated with colorectal carcinoma infilt ration depth, lymph node metastasis ; A negative correlation was observed between the expression of TβR Ⅱ and that of cyclinD1 ( P < 0. 05) . Conclusion  The overexpression of TGF2β1 was highly related to the invasion or metastasis of colorectal carcinoma ; Decreased expression of TβR Ⅱ was helpful not only to enhance cell growth resistance to TGF2β1 but increase the invasion of colorectal carcinoma ; cyclinD1 may played a role in the resistance of TGF-β1.

     

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