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在前列腺癌进展过程中,p14ARF、p15INK4b、p16INK4a和DCR2的表达增加。

Expression of p14ARF, p15INK4b, p16INK4a, and DCR2 increases during prostate cancer progression.

作者信息

Zhang Zhihong, Rosen Daniel G, Yao Jorge L, Huang Jiaoti, Liu Jinsong

机构信息

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030-4095, USA.

出版信息

Mod Pathol. 2006 Oct;19(10):1339-43. doi: 10.1038/modpathol.3800655. Epub 2006 Jun 23.

Abstract

Prostate carcinoma is a hormonally driven age-related neoplasm. Cellular senescence is an age-related process where cells remain metabolically active but in a growth-arrested state at the G1 phase. p14(ARF), p15(INK4b), and p16(INK4a), which are known to regulate G1 cell cycle arrest, and the tumor necrosis factor receptor superfamily member decoy receptor 2 (DCR2), have been recently identified as senescence markers. The purpose of this study was to characterize and compare the expression of p14(ARF), p15(INK4b), p16(INK4a), and DCR2 in tissue microarrays containing cases of normal prostate, nodular hyperplasia, prostate intraepithelial neoplasia (PIN), and malignant prostate cancer tissue. We performed immunohistochemical staining for p14(ARF), p15(INK4b), p16(INK4a), and DCR2 in tissue microarray blocks containing 41 cores of normal prostate, 65 cores of nodular hyperplasia, 21 cores of PIN, 69 cores of low-grade prostate carcinoma, and 42 cores of high-grade prostate carcinoma, derived from 80 cases of prostatectomy with adenocarcinomas. We detected positive staining of p16(INK4a) in 19% of the PIN, 25% of the low-grade carcinoma, and 43% of the high-grade carcinoma specimens but none in the normal prostate and nodular hyperplasia specimens. Expression of p14(ARF) revealed very high levels of expression in normal tissues (83%), nodular hyperplasia (88%), PIN (89%), and cancer cells (100%). P15(INK4b) and DCR2 were found positive in 81 and 33% normal, 46 and 10% nodular hyperplasia, 74 and 36% PIN tissues, 87 and 89% low-grade carcinomas, and 100 and 93% high-grade carcinomas. There is an increased protein expression of senescence-associated molecular markers, indicating that cellular senescence might play a role in prostate carcinoma. Because p16(INK4a)-positive cells were detected only in premalignant lesions and carcinomas but not in normal or benign tissues, p16(INK4a) may aid in the diagnosis of PIN and prostate cancer in difficult cases.

摘要

前列腺癌是一种激素驱动的与年龄相关的肿瘤。细胞衰老为一种与年龄相关的过程,在此过程中细胞保持代谢活性,但在G1期处于生长停滞状态。已知调节G1期细胞周期停滞的p14(ARF)、p15(INK4b)和p16(INK4a)以及肿瘤坏死因子受体超家族成员诱饵受体2(DCR2),最近已被鉴定为衰老标志物。本研究的目的是在包含正常前列腺、结节性增生、前列腺上皮内瘤变(PIN)和恶性前列腺癌组织病例的组织微阵列中,对p14(ARF)、p15(INK4b)、p16(INK4a)和DCR2的表达进行特征描述和比较。我们对包含41个正常前列腺组织芯、65个结节性增生组织芯、21个PIN组织芯、69个低级别前列腺癌组织芯和42个高级别前列腺癌组织芯的组织微阵列块进行了p14(ARF)、p15(INK4b)、p16(INK4a)和DCR2的免疫组织化学染色,这些组织芯来自80例前列腺腺癌切除术病例。我们在19%的PIN、25%的低级别癌和43%的高级别癌标本中检测到p16(INK4a)阳性染色,但在正常前列腺和结节性增生标本中未检测到。p14(ARF)的表达在正常组织(83%)、结节性增生(88%)、PIN(89%)和癌细胞(100%)中显示出非常高的表达水平。发现p15(INK4b)和DCR2在正常组织中阳性率分别为81%和33%,结节性增生中为46%和10%,PIN组织中为74%和36%,低级别癌中为87%和89%,高级别癌中为100%和93%。衰老相关分子标志物的蛋白表达增加,表明细胞衰老可能在前列腺癌中起作用。由于仅在癌前病变和癌组织中检测到p16(INK4a)阳性细胞,而在正常或良性组织中未检测到,因此p16(INK4a)可能有助于疑难病例中PIN和前列腺癌的诊断。

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