4.4 Article

Expression of B7-H4 and IDO1 is associated with drug resistance and poor prognosis in high-grade serous ovarian carcinomas

期刊

HUMAN PATHOLOGY
卷 113, 期 -, 页码 20-27

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.humpath.2021.04.003

关键词

B7-H4; IDO1; Ovarian carcinoma; Immunotherapy; Drug resistance

资金

  1. University of Texas MD Anderson Cancer Center SPORE grant [P50CA217685]
  2. MD Anderson Moonshot in Ovarian Cancer
  3. American Cancer Society
  4. Frank McGraw Memorial Chair in Cancer Research
  5. National Institutes of Health through MD Anderson's Cancer Center Support Grant [CA016672]

向作者/读者索取更多资源

The study identified high levels of immune modulatory proteins including B7-H4, IDO1, Tim3, IL-6, and IL-8 in high-grade serous ovarian carcinoma (HGSC), which were associated with therapy resistance and lower survival rates. These findings suggest novel targets for enhancing immunotherapy in HGSC patients, potentially improving treatment outcomes.
High-grade serous ovarian carcinoma (HGSC) is the most lethal gynecologic malignancy. While immune checkpoint inhibitors against PD-L1 and CTLA-4 have shown significant effects in multiple tumor types, the response rate to single-agent immune checkpoint inhibitors is low in HGSC. Alternative biomarkers and targets must be identified to guide patient selection and new therapeutic strategies in HGSC. Here, we aim to investigate the clinical significance of novel immune modulators, including B7-H4, IDO1, Tim3, IL6, and IL-8, in patients with HGSC. A total of 48 patients with HGSCs, comprising 24 cases that were sensitive and 24 that were resistant to standard paclitaxel and carboplatin chemotherapy, were selected for our initial analysis. A NanoString assay including 33 immune-related genes was used to compare the expression of different immune regulatory molecules in the sensitive and resistant groups. Differentially expressed proteins were verified using multiplex immunohistochemical staining on tissue arrays of 202 patients with HGSCs who underwent primary surgery at MDACC. We analyzed the expression levels of immune checkpoints and compared expression profiles with clinicopathologic features including response, progression-free survival, and overall survival. HGSC tumors resistant to therapy expressed higher levels of B7-H4 (69.3%), IDO1 (71.8%), Tim3 (89.1%), and inflammatory factors IL-6 and IL-8, and expressed higher Tim3 in stromal components. High expression of B7-H4 and IDO1 was associated with significantly lower overall survival and progression-free survival. B7-H4 and IDO1 were co-expressed in 49.1% of studied cases. A panel of immunomodulatory proteins including B7-H4, IDO1, Tim3, IL-6, and IL-8 are expressed at high levels in HGSCs. These modulators represent novel targets to enhance immunotherapy in patients with HGSCs. (C) 2021 Elsevier Inc. All rights reserved.

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