首页> 外文OA文献 >PD-L1, FGFR1, PIK3CA, PTEN, and p16 expression in pulmonary emphysema and chronic obstructive pulmonary disease with resected lung squamous cell carcinoma
【2h】

PD-L1, FGFR1, PIK3CA, PTEN, and p16 expression in pulmonary emphysema and chronic obstructive pulmonary disease with resected lung squamous cell carcinoma

机译:PD-L1,FGFR1,PIK3CA,PTEN和P16在肺气肿和慢性阻塞性肺病中表达,具有切除肺鳞状细胞癌

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Abstract Background Emphysema and chronic obstructive pulmonary disease (COPD) are well known independent risk factors for lung cancer. However, the developmental mechanisms between emphysema/COPD and lung cancer remain unknown. The purpose of this study was to evaluate PD-L1, FGFR1, PIK3CA, PTEN, and p16 expression in squamous cell carcinoma (SCC) associated with emphysema/COPD. Methods A total of 59 patients with squamous cell lung carcinoma (SCC) resected between 2008 and 2012 were retrospectively reviewed. Emphysema was assessed according to the Goddard score. Total severity was divided into none-mild (0–7), moderate (8–15), and severe (≥ 16). Local severity around the existing tumor was divided into no emphysema (0) and presence of emphysema (1–4). COPD severity was based on the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria. PD-L1, FGFR1, PIK3CA, PTEN, and p16 expression were evaluated by immunohistochemistry (IHC). Expression level was classified as tumor cells (TC) 3 (≥ 50%), TC2 (5–49%), TC1 (1–4%), or TC0 (< 1%), and as tumor-infiltrating immune cells (IC) 3 (≥ 50%), IC2 (5–49%), IC1 (1–4%), or IC0 (< 1%) for PD-L1. Expression level was compared between none-mild/moderate-severe total emphysema, no/presence of local emphysema, no COPD/COPD, and GOLD 1/GOLD 2, 3. Results PD-L1 expression was significantly correlated with severity of emphysema in TC0, 1, 2 vs. TC3 (P = 0.012). PD-L1 was significantly higher inversely in none-mild emphysema compared to moderate-severe (95% CI, 0.061–5.852, P = 0.045). There were no other significant associations between PD-L1, FGFR1, PIK3CA, PTEN, and p16 expression and total/local severity of emphysema or presence of COPD/GOLD stage. Conclusions PD-L1 expression in SCC was correlated with severity of emphysema in TC0, 1, 2 vs. TC3 and more frequent in none-mild emphysema than moderate-severe emphysema.
机译:抽象背景肺气肿和慢性阻塞性肺病(COPD)是公知的用于肺癌的独立危险因素。然而,肺气肿/ COPD和肺癌之间的发育机制尚不清楚。本研究的目的是评估PD-L1,FGFR1,PIK3CA,PTEN和p16蛋白的表达在与肺气肿/ COPD相关的鳞状细胞癌(SCC)。方法对59例2008年至2012年间手术切除肺鳞状细胞癌(SCC)进行回顾性分析。肺气肿是根据戈达德评分来评估。总的严重程度分为无,轻度(0-7),中度(8-15)和重度(≥16)。围绕现有肿瘤的局部严重程度分为无肺气肿(0)和肺气肿(1-4)的存在下进行。 COPD严重程度依据慢性阻塞性肺疾病(GOLD)标准的全球倡议。 PD-L1,FGFR1,PIK3CA,PTEN,和p16表达通过免疫组化(IHC)评估。表达水平被分类为肿瘤细胞(TC)3(≥50%),TC2(5-49%),TC1(1-4%),或TC0(<1%),和作为肿瘤浸润免疫细胞(IC )3(≥50%),IC2(5-49%),IC1(1-4%),或IC0(<1%)对PD-L1。表达水平之间进行比较无轻度/中度 - 重度总肺气肿,没有/本地肺气肿,慢性阻塞性肺病无/ COPD,和GOLD 1/2 GOLD,3.结果PD-L1表达的存在下显著与TC0肺气肿的严重程度相关,1,2与TC3(P = 0.012)。 PD-L1为显著更高成反比在相比中度 - 重度无轻度肺气肿(95%CI,0.061-5.852,P = 0.045)。有PD-L1,FGFR1,PIK3CA,PTEN和p16蛋白表达和总/肺气肿或慢性阻塞性肺病/ GOLD阶段的存在的本地严重性之间没有其它显著关联。在SCC结论PD-L1表达与TC0,1,2和肺气肿的严重程度与TC3比中度 - 重度肺气肿更频繁的在无轻度肺气肿相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号