Bombesin家族配体和受体在人胃癌组织和细胞系中的表达。

Yoon Kim, Hanhui Yang, S. Oh
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摘要

目的:bombesin样肽在许多小细胞肺癌细胞系的自分泌生长中起重要作用。本研究的目的是探讨bombesin家族配体/受体在人胃癌组织和细胞系中的表达程度,并探讨bombesin家族配体/受体的表达与临床病理参数的关系。方法:测定胃泌素释放肽(gstrin releasing peptide, GAP)、神经质素B (neuromedin B, NMB)及其受体在人胃癌组织和细胞系中的表达。对20例肿瘤和匹配的正常样本以及9株胃细胞系进行配体和受体mRNA的研究。逆转录聚合酶链反应(RT-PCR)检测GRP/NMB及其受体mRNA的表达。结果:GRP、NMB和GRPR、NMBR mRNA分别在55%、100%、40%和100%的胃癌组织中表达。30%的胃癌组织中可见GRP/GRPR共表达,胃癌组织中GRP/GRPR的表达高于正常粘膜。GRP和GRPR在分化型胃癌中高表达。在胃癌细胞系中,这些肽和受体表达相同。结论:GRP、NMB、GRPR、NMBR在胃癌组织和细胞系中均有表达。这一结果表明,这些肽可能在胃癌生长中发挥生长因子的作用,这些肽可能在胃癌中以自分泌方式作为形态形成因子。
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Expression of Bombesin Family Ligands and Receptors in Human Gastric Cancer Tissues and Cell Lines.
Purpose: Bombesin-like peptides are known to be important in the autocrine growth of a number of smlll cell lung cancer cell lines. The aim of this study was to investigate the extent of bombesin family ligands/receptors expression in human gastric cancer tissues and cell lines, and to evaluate the relationship between the expression of bombesin family Iigands/receptor and clinicopathologic parameters. Methods: We measured the expression of gstrin releasing peptide (GAP), neuromedin B (NMB), and their receptors, in human gastric cancer tissues and cell lines. Ligand and receptor mRNA studies were carried out on: 20 tumor and matched normal samples, and 9 gastric cell lines. The expression of mRNA of GRP/NMB, and their receptors, was examined by the reverse transcription-polymerase chain reaction (RT-PCR). Results: Expression of GRP, NMB and GRPR, NMBR mRNA was found in 55%, 100%, 40%, and 100% of gastric cancer tissue, respectively. GRP/GRPR co-expression was observed in 30% of gastric cancer tissues and expression of gastric cancer was higher than that of normal mucosa. GRP and GRPR were highly expressed in the differentiated type of gastric cancer. In gastric cancer cell lines, these peptides and receptors were expressed equally. Conclusion: The result demonstrate that GRP, NMB, GRPR, and NMBR were expressed in gastric cancer tissues and cell lines. This result suggests that these may have a role as growth factors in gastric cancer growth, and these peptides may act in an autocrine fashion as a morphogen in gastric cancer.
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