Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinoma

Abstract Failure of currently used cytotoxic chemotherapy is one of the main reasons behind high mortality from metastatic high grade serous ovarian carcinoma. We found that high expression of a receptor for fractalkine (CX3CR1) significantly correlated with shorter survival of patients with serous...

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Main Authors: Jia Xie, Hilal Gurler Main, Joelle D. Sacks, Goda G. Muralidhar, Maria V. Barbolina
Format: Article
Language:English
Published: Nature Publishing Group 2018-05-01
Series:Oncogenesis
Online Access:https://doi.org/10.1038/s41389-018-0046-6
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spelling doaj-f4d475cc4c374c4b860940b39eebbb022020-12-07T23:30:45ZengNature Publishing GroupOncogenesis2157-90242018-05-017511510.1038/s41389-018-0046-6Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinomaJia Xie0Hilal Gurler Main1Joelle D. Sacks2Goda G. Muralidhar3Maria V. Barbolina4Department of Biopharmaceutical Sciences, University of Illinois at ChicagoDepartment of Biopharmaceutical Sciences, University of Illinois at ChicagoDepartment of Biopharmaceutical Sciences, University of Illinois at ChicagoDepartment of Biopharmaceutical Sciences, University of Illinois at ChicagoDepartment of Biopharmaceutical Sciences, University of Illinois at ChicagoAbstract Failure of currently used cytotoxic chemotherapy is one of the main reasons behind high mortality from metastatic high grade serous ovarian carcinoma. We found that high expression of a receptor for fractalkine (CX3CR1) significantly correlated with shorter survival of patients with serous ovarian carcinoma treated with cytotoxic DNA damage chemotherapies, and reduction of CX3CR1 expression resulted in sensitization to several DNA damaging modalities, including x-ray radiation and cisplatin. Here, we show that CX3CR1 plays a role in double-strand DNA break response and repair by regulating expression of RAD50 by a MYC-dependent mechanism. We demonstrate that downregulation of CX3CR1 alone and in a combination with irradiation affects peritoneal metastasis in an organ-specific manner; we show that CX3CR1 regulates lipid uptake which could control omental metastasis. This study identifies CX3CR1 as a novel potential target for sensitization of ovarian carcinoma to DNA damage therapies and reduction of peritoneal carcinomatosis.https://doi.org/10.1038/s41389-018-0046-6
collection DOAJ
language English
format Article
sources DOAJ
author Jia Xie
Hilal Gurler Main
Joelle D. Sacks
Goda G. Muralidhar
Maria V. Barbolina
spellingShingle Jia Xie
Hilal Gurler Main
Joelle D. Sacks
Goda G. Muralidhar
Maria V. Barbolina
Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinoma
Oncogenesis
author_facet Jia Xie
Hilal Gurler Main
Joelle D. Sacks
Goda G. Muralidhar
Maria V. Barbolina
author_sort Jia Xie
title Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinoma
title_short Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinoma
title_full Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinoma
title_fullStr Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinoma
title_full_unstemmed Regulation of DNA damage repair and lipid uptake by CX3CR1 in epithelial ovarian carcinoma
title_sort regulation of dna damage repair and lipid uptake by cx3cr1 in epithelial ovarian carcinoma
publisher Nature Publishing Group
series Oncogenesis
issn 2157-9024
publishDate 2018-05-01
description Abstract Failure of currently used cytotoxic chemotherapy is one of the main reasons behind high mortality from metastatic high grade serous ovarian carcinoma. We found that high expression of a receptor for fractalkine (CX3CR1) significantly correlated with shorter survival of patients with serous ovarian carcinoma treated with cytotoxic DNA damage chemotherapies, and reduction of CX3CR1 expression resulted in sensitization to several DNA damaging modalities, including x-ray radiation and cisplatin. Here, we show that CX3CR1 plays a role in double-strand DNA break response and repair by regulating expression of RAD50 by a MYC-dependent mechanism. We demonstrate that downregulation of CX3CR1 alone and in a combination with irradiation affects peritoneal metastasis in an organ-specific manner; we show that CX3CR1 regulates lipid uptake which could control omental metastasis. This study identifies CX3CR1 as a novel potential target for sensitization of ovarian carcinoma to DNA damage therapies and reduction of peritoneal carcinomatosis.
url https://doi.org/10.1038/s41389-018-0046-6
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