Zheng Mingjun, Long Junyu, Chelariu-Raicu Anca, Mullikin Heather, Vilsmaier Theresa, Vattai Aurelia, Heidegger Helene Hildegard, Batz Falk, Keckstein Simon, Jeschke Udo, Trillsch Fabian, Mahner Sven, Kaltofen Till
Department of Obstetrics and Gynecology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377 Munich, Germany.
Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan 3rd Alley, Dongcheng District, Beijing 100730, China.
Cancers (Basel). 2021 Jul 3;13(13):3343. doi: 10.3390/cancers13133343.
(1) Background: The tumor microenvironment is involved in the growth and proliferation of malignant tumors and in the process of resistance towards systemic and targeted therapies. A correlation between the gene expression profile of the tumor microenvironment and the prognosis of ovarian cancer patients is already known. (2) Methods: Based on data from The Cancer Genome Atlas (379 RNA sequencing samples), we constructed a prognostic 11-gene signature (, , , , , , , , , and ) for Fédération Internationale de Gynécologie et d'Obstétrique stage III and IV serous ovarian cancer through lasso regression. (3) Results: The established risk score was able to predict the 1-, 3- and 5-year prognoses more accurately than previously known models. (4) Conclusions: We were able to confirm the predictive power of this model when we applied it to cervical and urothelial cancer, supporting its pan-cancer usability. We found that immune checkpoint genes correlate negatively with a higher risk score. Based on this information, we used our risk score to predict the biological response of cancer samples to an anti-programmed death ligand 1 immunotherapy, which could be useful for future clinical studies on immunotherapy in ovarian cancer.
(1) 背景:肿瘤微环境参与恶性肿瘤的生长和增殖以及对全身治疗和靶向治疗的抵抗过程。肿瘤微环境的基因表达谱与卵巢癌患者预后之间的相关性已为人所知。(2) 方法:基于癌症基因组图谱的数据(379个RNA测序样本),我们通过套索回归构建了国际妇产科联盟III期和IV期浆液性卵巢癌的预后11基因特征(、、、、、、、、、和)。(3) 结果:所建立的风险评分比先前已知模型更准确地预测1年、3年和5年预后。(4) 结论:当我们将该模型应用于宫颈癌和尿路上皮癌时,能够证实其预测能力,支持其泛癌实用性。我们发现免疫检查点基因与较高的风险评分呈负相关。基于此信息,我们使用风险评分预测癌症样本对程序性死亡配体1免疫疗法的生物学反应,这可能对未来卵巢癌免疫治疗的临床研究有用。