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p27(Kip1) expression as a prognostic marker for squamous cell carcinoma of the head and neck (Review)

机译:p27(Kip1)表达可作为头颈部鳞状细胞癌的预后标志物(综述)

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摘要

Regulation of the cell cycle is essential for carcinogenesis. The cell cycle is controlled by cyclin-dependent kinases (CDKs), which are upregulated by cyclins and downregulated by CDK inhibitors (CDKIs). Decreased p27(Kip1) expression has been associated with survival rate, tumor size, histological differentiation and the presence of lymph node metastasis in patients with various types of cancer. The aim of the current study is to provide a literature review on the association between p27(Kip1) expression and the clinical and pathological aspects of head and neck squamous cell carcinoma (HNSCC), and the expression of other CDKIs of the Cip/Kip family and cyclins. Throughout the literature, different methodologies were used to determine the immunohistochemical expression of p27(Kip1); thus, results concerning p27(Kip1) expression in HNSCC vary widely. However, it has now been confirmed that p27(Kip1) is underexpressed in SCC cells. p27 may be a promising marker for determining the prognosis of HNSCC, despite the marked variability of the results obtained. An association between p27 expression and survival rate, time to recurrence and tumor stage has been observed. Based on the information currently available, it is premature to recommend the analysis of p27(Kip1) expression in guiding HNSCC treatment planning. However, although relatively unstudied, the correlation between p27(Kip1) expression and other tumor suppressor genes may turn out to be important in determining the prognosis of HNSCC. Further prospective studies utilizing standardized laboratory methodologies and statistics that facilitate meta-analyses are required to confirm this proposal.
机译:细胞周期的调节对于致癌至关重要。细胞周期受细胞周期蛋白依赖性激酶(CDK)的控制,而细胞周期蛋白依赖性激酶(CDKs)则由细胞周期蛋白上调,而CDK抑制剂(CDKIs)下调。 p27(Kip1)表达下降与各种类型癌症患者的存活率,肿瘤大小,组织学分化和淋巴结转移的存在有关。本研究的目的是提供有关p27(Kip1)表达与头颈部鳞状细胞癌(HNSCC)的临床和病理方面以及Cip / Kip家族其他CDKIs表达之间的关联的文献综述和细胞周期蛋白。在整个文献中,使用不同的方法来确定p27(Kip1)的免疫组织化学表达。因此,有关HNSCC中p27(Kip1)表达的结果差异很大。但是,现在已经证实p27(Kip1)在SCC细胞中表达不足。尽管获得的结果存在明显差异,但p27可能是确定HNSCC预后的有前途的标志物。已经观察到p27表达与存活率,复发时间和肿瘤阶段之间存在关联。根据目前可用的信息,建议对p27(Kip1)表达进行分析以指导HNSCC治疗计划为时尚早。然而,尽管相对未被研究,但p27(Kip1)表达与其他肿瘤抑制基因之间的相关性可能对确定HNSCC的预后至关重要。需要进一步的利用标准化实验室方法和统计数据的前瞻性研究来促进荟萃分析,以确认该提议。

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