Long Long, Chen Mengxi, Yuan Yu, Ming Alex Lau, Guo Wei, Wu Kaisong, Chen Honglei
Department of Pathology, Zhongnan Hospital of Wuhan University, Wuhan 430071, P. R. China.
Department of Pathology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, P. R. China.
J Cancer. 2020 May 18;11(15):4442-4452. doi: 10.7150/jca.42610. eCollection 2020.
: Immunotherapy targeting PD-1/PD-L1 represents a breakthrough in the treatment of lung cancer. Pyruvate kinase M2 (PKM2) is not only a critical player in glycolysis, but also conducive to tumor progression and immune response. While both have been linked to lung adenocarcinoma (AC), the correlation and clinical significance of PKM2 and PD-L1 expression in human lung AC tissues remains not entirely explored. : Expression of PKM2 and PD-L1 proteins were detected by immunohistochemistry in 74 lung AC cases and the corresponding noncancerous tissues. Simultaneously, multiplex immunofluorescence was used to detect PKM2, PD-L1, CK, CD3, and CD68 in the lung AC tissues. We measured expression patterns and co-localization of these markers, evaluating their association with clinicopathological features and overall survival. Validation of findings was conducted using mRNA expression data from The Cancer Genome Atlas (TCGA) of 515 lung AC cases. : High expression of PKM2 in tumor cells was significantly related with lymph node metastasis and TNM stage (p=0.035, p=0.017, respectively). Moreover, PKM2 expression in tumor cells was positively correlated with tumor PD-L1 expression. High expression of PKM2, PD-L1 in tumor cells and immune cells predicted high mortality rate and poorer survival rates, respectively. Additionally, multivariate Cox regression models indicated that high expression of PKM2 in tumor cells was an independent prognostic factor. Based on TCGA genomic data, high PKM2 mRNA expression was significantly associated with poorer survival (p=0.001). : High expression of PKM2 synergizes with PD-L1 in tumor cells and immune cells to predict poorer survival rates in patients with lung AC.
针对PD-1/PD-L1的免疫疗法是肺癌治疗的一项突破。丙酮酸激酶M2(PKM2)不仅是糖酵解中的关键因子,还有助于肿瘤进展和免疫反应。虽然两者都与肺腺癌(AC)有关,但PKM2与PD-L1在人肺AC组织中的表达相关性及临床意义仍未完全明确。
通过免疫组织化学检测74例肺AC病例及相应癌旁组织中PKM2和PD-L1蛋白的表达。同时,采用多重免疫荧光法检测肺AC组织中的PKM2、PD-L1、细胞角蛋白(CK)、CD3和CD68。我们测量了这些标志物的表达模式和共定位情况,评估它们与临床病理特征及总生存期的相关性。利用来自515例肺AC病例的癌症基因组图谱(TCGA)的mRNA表达数据对研究结果进行验证。
肿瘤细胞中PKM2的高表达与淋巴结转移和TNM分期显著相关(分别为p = 0.035,p = 0.017)。此外,肿瘤细胞中PKM2的表达与肿瘤PD-L1的表达呈正相关。肿瘤细胞和免疫细胞中PKM2、PD-L1的高表达分别预示着高死亡率和较差的生存率。此外,多因素Cox回归模型表明肿瘤细胞中PKM2的高表达是一个独立的预后因素。基于TCGA基因组数据,PKM2 mRNA高表达与较差的生存率显著相关(p = 0.001)。
肿瘤细胞和免疫细胞中PKM2的高表达与PD-L1协同作用,预示肺AC患者生存率较差。