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Expression of Telomerase Activity, Human Telomerase RNA, and Telomerase Reverse Transcriptase in Gastric Adenocarcinomas

机译:胃腺癌中端粒酶活性,人类端粒酶RNA和端粒酶逆转录酶的表达

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Telomerase is an RNA-dependent DNA polymerase that synthesizes TTAGGG telomeric DNA onto chromosome ends to compensate for sequence loss during DNA replication. It has been detected in 85–90% of all primary human cancers, implicating that the telomerase seems to be reactivated in tumors and that such activity may play a role in the tumorigenic process. The purpose of this study was to evaluate telomerase activity, human telomerase RNA (hTR), and telomerase reverse transcriptase (TERT) in stomach cancer and to determine their potential relationships to clinicopathologic parameters. Frozen and corresponding methacarn-fixed paraffin-embedded tissue samples were obtained from 51 patients with gastric adenocarcinoma and analyzed for telomerase activity by using a TRAPeze ELISA kit. Tissue sections of all the samples were further investigated for hTR and TERT by in situ hybridization and a sensitive immunohistochemical technique, respectively. Telomerase activity was detected in 37 (73%) tumors. Telomerase positivity from methacarn-fixed paraffin blocks was found to be 35% of that from frozen tissues. hTR was overexpressed in 46 (90%) samples: 33/37 (89%) with and 13/14 (93%) without telomerase activation. Expression of TERT was demonstrated in 40 (78%) cases: 30/37 (81%) with and 10/14 (71%) without telomerase. Telomerase activity correlated well with depth of invasion (P = .037) and tumor differentiation (P = .022), whereas hTR significantly correlated with nodal metastasis (P = .047) and tumor size (P = .023). These data suggest that reactivated telomerase may play a significant role in the tumorigenesis of gastric cancer and may reflect, along with enhanced hTR, the malignant potential of the tumor. It is noteworthy that methacarn-fixed tissue cannot as yet substitute for the frozen section in the TRAP assay.
机译:端粒酶是一种RNA依赖性DNA聚合酶,可将TTAGGG端粒DNA合成到染色体末端,以补偿DNA复制过程中的序列丢失。在所有原发性人类癌症中,有85%至90%的人检测到了这种现象,这表明端粒酶似乎在肿瘤中被重新激活,并且这种活性可能在致瘤过程中起作用。这项研究的目的是评估胃癌中的端粒酶活性,人类端粒酶RNA(hTR)和端粒酶逆转录酶(TERT),并确定它们与临床病理参数的潜在关系。从51例胃腺癌患者中获取冷冻的和相应的美沙芬固定石蜡包埋的组织样品,并使用TRAPeze ELISA试剂盒分析端粒酶活性。通过原位杂交和灵敏的免疫组织化学技术分别对所有样品的组织切片进行hTR和TERT研究。在37个(73%)肿瘤中检测到端粒酶活性。发现美沙酮固定的石蜡块的端粒酶阳性率是冷冻组织的端粒酶阳性率的35%。 hTR在46个(90%)样品中过表达:33/37(89%)有和没有端粒酶激活的13/14(93%)。在40(78%)的情况下证明了TERT的表达:有端粒酶的情况下为30/37(81%),无端粒酶的情况下为10/14(71%)。端粒酶活性与浸润深度(P = .037)和肿瘤分化(P = .022)密切相关,而hTR与淋巴结转移(P = .047)和肿瘤大小(P = .023)密切相关。这些数据表明,重新激活的端粒酶可能在胃癌的肿瘤发生中起重要作用,并且可能与hTR的增强一起反映出肿瘤的恶性潜能。值得注意的是,美卡康固定的组织尚不能替代TRAP分析中的冷冻切片。

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