Activation-Induced Cytidine Deaminase Links Ovulation-Induced Inflammation and Serous Carcinogenesis

Stav Sapoznik; Keren Bahar-Shany; Yishay Pinto; Orshay Gabay; Efrat Glick-Saar; Chen Dor; Oranit Zadok; Iris Barshack; Adi Zundelevich; Einav Nili Gal-Yam; Yuval Yung; Ariel Hourvitz; Jacob Korach; Jasmine Jacob; Erez Y. Levanon; Michal Barak; Sarit Aviel-Ronen

doi:https://doi.org/10.1016/j.neo.2015.12.003

Activation-Induced Cytidine Deaminase Links Ovulation-Induced Inflammation and Serous Carcinogenesis

Stav Sapoznik, Keren Bahar-Shany, Yishay Pinto, Orshay Gabay, Efrat Glick-Saar, Chen Dor, Oranit Zadok, Iris Barshack, Adi Zundelevich, Einav Nili Gal-Yam, Yuval Yung, Ariel Hourvitz, Jacob Korach, Jasmine Jacob, Erez Y. Levanon, Michal Barak, Sarit Aviel-Ronen

The Mina and Everard Goodman Faculty of Life Sciences

Bar-Ilan University

Research output: Contribution to journal › Article › peer-review

Abstract

In recent years, the notion that ovarian carcinoma results from ovulation-induced inflammation of the fallopian tube epithelial cells (FTECs) has gained evidence. However, the mechanistic pathway for this process has not been revealed yet. In the current study, we propose the mutator protein activation-induced cytidine deaminase (AID) as a link between ovulation-induced inflammation in FTECs and genotoxic damage leading to ovarian carcinogenesis. We show that AID, previously shown to be functional only in B lymphocytes, is expressed in FTECs under physiological conditions, and is induced in vitro upon ovulatory-like stimulation and in vivo in carcinoma-associated FTECs. We also report that AID activity results in epigenetic, genetic and genomic damage in FTECs. Overall, our data provides new insights into the etiology of ovarian carcinogenesis and may set the ground for innovative approaches aimed at prevention and early detection.

Original language	English
Pages (from-to)	90-99
Number of pages	10
Journal	Neoplasia (United States)
Volume	18
Issue number	2
DOIs	https://doi.org/10.1016/j.neo.2015.12.003
State	Published - Feb 2016

All Science Journal Classification (ASJC) codes

Cancer Research

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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https://doi.org/10.1016/j.neo.2015.12.003

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Sapoznik, S., Bahar-Shany, K., Pinto, Y., Gabay, O., Glick-Saar, E., Dor, C., Zadok, O., Barshack, I., Zundelevich, A., Gal-Yam, E. N., Yung, Y., Hourvitz, A., Korach, J., Jacob, J., Levanon, E. Y., Barak, M., & Aviel-Ronen, S. (2016). Activation-Induced Cytidine Deaminase Links Ovulation-Induced Inflammation and Serous Carcinogenesis. Neoplasia (United States), 18(2), 90-99. https://doi.org/10.1016/j.neo.2015.12.003

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title = "Activation-Induced Cytidine Deaminase Links Ovulation-Induced Inflammation and Serous Carcinogenesis",

abstract = "In recent years, the notion that ovarian carcinoma results from ovulation-induced inflammation of the fallopian tube epithelial cells (FTECs) has gained evidence. However, the mechanistic pathway for this process has not been revealed yet. In the current study, we propose the mutator protein activation-induced cytidine deaminase (AID) as a link between ovulation-induced inflammation in FTECs and genotoxic damage leading to ovarian carcinogenesis. We show that AID, previously shown to be functional only in B lymphocytes, is expressed in FTECs under physiological conditions, and is induced in vitro upon ovulatory-like stimulation and in vivo in carcinoma-associated FTECs. We also report that AID activity results in epigenetic, genetic and genomic damage in FTECs. Overall, our data provides new insights into the etiology of ovarian carcinogenesis and may set the ground for innovative approaches aimed at prevention and early detection.",

author = "Stav Sapoznik and Keren Bahar-Shany and Yishay Pinto and Orshay Gabay and Efrat Glick-Saar and Chen Dor and Oranit Zadok and Iris Barshack and Adi Zundelevich and Gal-Yam, {Einav Nili} and Yuval Yung and Ariel Hourvitz and Jacob Korach and Jasmine Jacob and Levanon, {Erez Y.} and Michal Barak and Sarit Aviel-Ronen",

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year = "2016",

month = feb,

doi = "https://doi.org/10.1016/j.neo.2015.12.003",

language = "الإنجليزيّة",

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Sapoznik, S, Bahar-Shany, K, Pinto, Y, Gabay, O, Glick-Saar, E, Dor, C, Zadok, O, Barshack, I, Zundelevich, A, Gal-Yam, EN, Yung, Y, Hourvitz, A, Korach, J, Jacob, J, Levanon, EY, Barak, M & Aviel-Ronen, S 2016, 'Activation-Induced Cytidine Deaminase Links Ovulation-Induced Inflammation and Serous Carcinogenesis', Neoplasia (United States), vol. 18, no. 2, pp. 90-99. https://doi.org/10.1016/j.neo.2015.12.003

TY - JOUR

T1 - Activation-Induced Cytidine Deaminase Links Ovulation-Induced Inflammation and Serous Carcinogenesis

AU - Sapoznik, Stav

AU - Bahar-Shany, Keren

AU - Pinto, Yishay

AU - Gabay, Orshay

AU - Glick-Saar, Efrat

AU - Dor, Chen

AU - Zadok, Oranit

AU - Barshack, Iris

AU - Zundelevich, Adi

AU - Gal-Yam, Einav Nili

AU - Yung, Yuval

AU - Hourvitz, Ariel

AU - Korach, Jacob

AU - Jacob, Jasmine

AU - Levanon, Erez Y.

AU - Barak, Michal

AU - Aviel-Ronen, Sarit

PY - 2016/2

Y1 - 2016/2

N2 - In recent years, the notion that ovarian carcinoma results from ovulation-induced inflammation of the fallopian tube epithelial cells (FTECs) has gained evidence. However, the mechanistic pathway for this process has not been revealed yet. In the current study, we propose the mutator protein activation-induced cytidine deaminase (AID) as a link between ovulation-induced inflammation in FTECs and genotoxic damage leading to ovarian carcinogenesis. We show that AID, previously shown to be functional only in B lymphocytes, is expressed in FTECs under physiological conditions, and is induced in vitro upon ovulatory-like stimulation and in vivo in carcinoma-associated FTECs. We also report that AID activity results in epigenetic, genetic and genomic damage in FTECs. Overall, our data provides new insights into the etiology of ovarian carcinogenesis and may set the ground for innovative approaches aimed at prevention and early detection.

AB - In recent years, the notion that ovarian carcinoma results from ovulation-induced inflammation of the fallopian tube epithelial cells (FTECs) has gained evidence. However, the mechanistic pathway for this process has not been revealed yet. In the current study, we propose the mutator protein activation-induced cytidine deaminase (AID) as a link between ovulation-induced inflammation in FTECs and genotoxic damage leading to ovarian carcinogenesis. We show that AID, previously shown to be functional only in B lymphocytes, is expressed in FTECs under physiological conditions, and is induced in vitro upon ovulatory-like stimulation and in vivo in carcinoma-associated FTECs. We also report that AID activity results in epigenetic, genetic and genomic damage in FTECs. Overall, our data provides new insights into the etiology of ovarian carcinogenesis and may set the ground for innovative approaches aimed at prevention and early detection.

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DO - https://doi.org/10.1016/j.neo.2015.12.003

M3 - مقالة

C2 - 26936395

SN - 1522-8002

VL - 18

SP - 90

EP - 99

JO - Neoplasia (United States)

JF - Neoplasia (United States)

IS - 2

ER -

Activation-Induced Cytidine Deaminase Links Ovulation-Induced Inflammation and Serous Carcinogenesis

Abstract

All Science Journal Classification (ASJC) codes

UN SDGs

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