基质细胞衍生因子1-α促进结直肠癌的肿瘤进展。

Se Jun Park, Tae Sung Ahn, Sung Woo Cho, Chang Jin Kim, Dong Jun Jung, Myung Won Son, Sang Ho Bae, Eung Jin Shin, Moon Soo Lee, Chang Ho Kim, Moo Jun Baek
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引用次数: 3

摘要

目的:虽然基质细胞衍生因子(SDF)-1α被认为参与肿瘤发生和肿瘤血管生成,但其在结直肠癌中的表达的临床病理意义尚不完全清楚。我们检测了SDF-1α在结直肠癌中的表达,并探讨了其与肿瘤分期、淋巴结转移、血管侵袭(VI)、淋巴侵袭(LI)和神经侵袭(NI)等临床病理特征的关系。方法:对83例原发性结直肠癌标本进行免疫组化检查,分析临床病理特征与SDF-1α表达的关系。为了比较正常结肠组织和结直肠癌组织的表达,我们进行了Western blot分析。结果:Western blot结果显示,SDF-1α在结直肠癌组织中的表达高于正常结肠黏膜(20/21)。免疫组化染色显示,SDF-1α与淋巴结状态、远处转移、肿瘤分期、VI和LI相关。SDF-1α表达对总生存有显著的预后价值。高SDF-1α患者的Kaplan-Meier生存图显示,高SDF-1α表达与较短的总生存期相关。然而,没有发现SDF-1α表达与其他病理或临床变量(包括年龄、性别、分化程度和有无神经周围浸润)之间的关联。结论:SDF-1α的表达可能与结直肠癌的肿瘤进展有关。抑制SDF-1α可能是结直肠癌患者的一种治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stromal-cell-derived Factor 1-α Promotes Tumor Progression in Colorectal Cancer.

Stromal-cell-derived Factor 1-α Promotes Tumor Progression in Colorectal Cancer.

Stromal-cell-derived Factor 1-α Promotes Tumor Progression in Colorectal Cancer.

Stromal-cell-derived Factor 1-α Promotes Tumor Progression in Colorectal Cancer.

Purpose: Although stromal-cell-derived factor (SDF)-1α is suggested to be involved in tumorigenicity and tumor angiogenesis, the clinicopathological significance of its expression in colorectal cancers is not fully understood. We examined SDF-1α expression in colorectal cancers and investigated its relationship to clinicopathological features such as tumor staging, lymph-node metastasis, vascular invasion (VI), lymphatic invasion (LI) and neural invasion (NI).

Methods: Specimens of 83 primary colorectal cancers were examined immunohistochemically, and the relationships between clinicopathological features and SDF-1α expression were analyzed. To compare the expressions between the normal colon tissue and colorectal cancer tissues, we performed Western blot analyses.

Results: According to the Western blot analyses, SDF-1α was more highly expressed in colorectal carcinoma tissues than in normal colonic mucosa (20/21). According to the immunohistochemical stain, SDF-1α was associated with nodal status, distant metastasis, tumor staging, VI and LI. SDF-1α expression had a significant prognostic value for overall survival. Kaplan-Meier plots of survival in patients with high SDF-1α showed that high SDF-1α expression was associated with a shorter overall survival. However, no association was found between SDF-1α expression and other pathologic or clinical variables, including age, gender, degree of differentiation, and presence of perineural invasion.

Conclusion: The expression of SDF-1α might be associated with tumor progression in colorectal cancer. Inhibition of SDF-1α could be a therapeutic option in colorectal cancer patients.

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