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Up-regulation of PKM2 promote malignancy and related to adverse prognostic risk factor in human gallbladder cancer

机译:PKM2的上调促进恶性肿瘤并与人胆囊癌的不良预后危险因素有关

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摘要

Recently, pyruvate kinase M2 (PKM2) has been implicated in the progression of certain cancers and might play pivotal roles in the formation of malignancy. However, the role of PKM2 in gallbladder cancer had not been well investigated. This study analyzed associations between PKM2 expression status with various clinical and pathologic parameters in a large cohort of gallbladder cancer (GBC) patients from a long term follow up results. The expression level of pyruvate kinase isotypes in GBC tissues and their adjacent normal gallbladder tissues were estimated by qRT-PCR and Western blot. PKM2 mRNA level were significantly high in gallbladder cancer tissues than in adjacent noncancerous tissues (P < 0.001). High expression of the PKM2 was detected in 55.71% paraffin-embedded GBC tissue. The high PKM2 expression was independently associated with poorer overall survival in patients with GBC (median survival 11.9 vs 30.1 months; hazard ratio 2.79; 95% CI = 1.18 to 6.55; P = 0.02). These findings indicated elevated expression of PKM2 is a prognostic factor for poor GBC clinical outcomes, implied involving of PKM2 in GBC progression.
机译:最近,丙酮酸激酶M2(PKM2)与某些癌症的发展有关,可能在恶性肿瘤的形成中起关键作用。然而,PKM2在胆囊癌中的作用尚未得到很好的研究。这项研究从长期随访结果中分析了一大批胆囊癌(GBC)患者的PKM2表达状态与各种临床和病理参数之间的关联。通过qRT-PCR和Western blot检测GBC组织及其邻近正常胆囊组织中丙酮酸激酶同种型的表达水平。胆囊癌组织中PKM2 mRNA水平显着高于邻近的非癌组织(P <0.001)。在55.71%的石蜡包埋的GBC组织中检测到PKM2的高表达。 PKM2的高表达与GBC患者的整体生存较差独立相关(中位生存期为11.9个月对30.1个月;危险比为2.79; 95%CI = 1.18至6.55; P = 0.02)。这些发现表明,PKM2的升高表达是GBC临床预后不良的预后因素,这意味着PKM2参与了GBC进展。

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