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瘦素和瘦素受体在结肠癌组织中的表达及瘦素对结肠癌细胞株HT-29增殖及凋亡的影响[J]. 肿瘤防治研究, 2015, 42(01): 48-51. DOI: 10.3971/j.issn.1000-8578.2015.01.012
引用本文: 瘦素和瘦素受体在结肠癌组织中的表达及瘦素对结肠癌细胞株HT-29增殖及凋亡的影响[J]. 肿瘤防治研究, 2015, 42(01): 48-51. DOI: 10.3971/j.issn.1000-8578.2015.01.012
Expression of Leptin and Leptin Receptor in Colon Cancer and Impact of Exogenous Leptin on Proliferation and Apoptosis of Colon Cancer Cell Line HT-29[J]. Cancer Research on Prevention and Treatment, 2015, 42(01): 48-51. DOI: 10.3971/j.issn.1000-8578.2015.01.012
Citation: Expression of Leptin and Leptin Receptor in Colon Cancer and Impact of Exogenous Leptin on Proliferation and Apoptosis of Colon Cancer Cell Line HT-29[J]. Cancer Research on Prevention and Treatment, 2015, 42(01): 48-51. DOI: 10.3971/j.issn.1000-8578.2015.01.012

瘦素和瘦素受体在结肠癌组织中的表达及瘦素对结肠癌细胞株HT-29增殖及凋亡的影响

Expression of Leptin and Leptin Receptor in Colon Cancer and Impact of Exogenous Leptin on Proliferation and Apoptosis of Colon Cancer Cell Line HT-29

  • 摘要: 探讨瘦素和瘦素受体在结肠癌组织中的表达及其与结肠癌临床病理特征的关系,及外源性瘦素对结肠癌细胞株HT-29细胞增殖、凋亡的影响。方法 采用流式细胞分析仪检测瘦素和瘦素受体在结肠癌组织中的表达情况;MTT法和流式细胞分析仪检测外源性瘦素对结肠癌细胞株HT-29细胞生长、凋亡及细胞周期的影响。结果 瘦素在结肠癌及正常肠黏膜组织中的阳性表达率分别为(80.30±1.83)%和(59.83±1.12)%,差异具有统计学意义(P<0.01);瘦素受体在结肠癌及正常肠黏膜组织中的阳性表达率分别为(82.14±1.63)%和(65.21±1.45)%,差异具有统计学意义(P<0.05)。结肠癌组织中瘦素和瘦素受体的表达与结肠癌患者的性别、年龄、肿瘤分化程度、淋巴结、远处转移及临床分期无相关性(P>0.05)。浓度为50、100和200 ng/ml的外源性瘦素可明显促进结肠癌细胞株HT-29细胞的增殖(P<0.05),细胞在S期累积明显(P<0.05),但对HT-29细胞的凋亡无明显影响(P>0.05)。结论 瘦素和瘦素受体可能通过促进细胞增殖的方式在结肠癌发生过程中发挥重要作用。

     

    Abstract: Objective To investigate the expression of leptin and its receptor in human colon cancer, the relationship between their expression and clinicopathological parameters, and the impact of exogenous leptin on the proliferation and apoptosis of colon cancer cell line HT-29. Methods Flow cytometry was used to detect the expression of leptin and its receptor in human colon cancer. MTT assay and flow cytometry were used to detect exogenous leptin on the proliferation, apoptosis and cell cycle of colon cancer cell line HT-29. Results The expression of leptin in human colon cancer and normal intestinal mucosa were (80.30±1.83)% and (59.83±1.12)% (P<0.01); the expression of leptin receptor in human colon cancer and normal intestinal mucosa were (82.14±1.63)% and (65.21±1.45)% (P<0.05). There was no correlation between their expression and patient's age, gender, tumor differentiated degree, lymph node, distance metastasis or clinical stage (P>0.05). Concentration of 50, 100 and 200ng/ml exogenous leptin had a growing role in stimulating the proliferation of colon cancer cell line HT-29 (P<0.05). Cells were accumulated in S phase (P<0.05), but there was no difference in the apoptosis of HT-29 cells (P>0.05). Conclusion Leptin and its receptor may play an important role in human colon tumorgenesis through accelerating cell proliferation.

     

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