Fetal radiation exposure induces testicular cancer in genetically susceptible mice.

The prevalence of testicular germ cell tumors (TGCT), a common solid tissue malignancy in young men, has been annually increasing at an alarming rate of 3%. Since the majority of testicular cancers are derived from germ cells at the stage of transformation of primordial germ cell (PGC) into gonocyte...

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Main Authors: Gunapala Shetty, Paul B Comish, Connie C Y Weng, Angabin Matin, Marvin L Meistrich
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3278464?pdf=render
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spelling doaj-40a79151ed0c4f90b30583e0ab64c2322020-11-25T01:48:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0172e3206410.1371/journal.pone.0032064Fetal radiation exposure induces testicular cancer in genetically susceptible mice.Gunapala ShettyPaul B ComishConnie C Y WengAngabin MatinMarvin L MeistrichThe prevalence of testicular germ cell tumors (TGCT), a common solid tissue malignancy in young men, has been annually increasing at an alarming rate of 3%. Since the majority of testicular cancers are derived from germ cells at the stage of transformation of primordial germ cell (PGC) into gonocytes, the increase has been attributed to maternal/fetal exposures to environmental factors. We examined the effects of an estrogen (diethylstilbestrol, DES), an antiandrogen (flutamide), or radiation on the incidence of testicular germ cell tumors in genetically predisposed 129.MOLF-L1 (L1) congenic mice by exposing them to these agents on days 10.5 and 11.5 of pregnancy. Neither flutamide nor DES produced noticeable increases in testis cancer incidence at 4 weeks of age. In contrast, two doses of 0.8-Gy radiation increased the incidence of TGCT from 45% to 100% in the offspring. The percentage of mice with bilateral tumors, weights of testes with TGCT, and the percentage of tumors that were clearly teratomas were higher in the irradiated mice than in controls, indicating that irradiation induced more aggressive tumors and/or more foci of initiation sites in each testis. This radiation dose did not disrupt spermatogenesis, which was qualitatively normal in tumor-free testes although they were reduced in size. This is the first proof of induction of testicular cancer by an environmental agent and suggests that the male fetus of women exposed to radiation at about 5-6 weeks of pregnancy might have an increased risk of developing testicular cancer. Furthermore, it provides a novel tool for studying the molecular and cellular events of testicular cancer pathogenesis.http://europepmc.org/articles/PMC3278464?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Gunapala Shetty
Paul B Comish
Connie C Y Weng
Angabin Matin
Marvin L Meistrich
spellingShingle Gunapala Shetty
Paul B Comish
Connie C Y Weng
Angabin Matin
Marvin L Meistrich
Fetal radiation exposure induces testicular cancer in genetically susceptible mice.
PLoS ONE
author_facet Gunapala Shetty
Paul B Comish
Connie C Y Weng
Angabin Matin
Marvin L Meistrich
author_sort Gunapala Shetty
title Fetal radiation exposure induces testicular cancer in genetically susceptible mice.
title_short Fetal radiation exposure induces testicular cancer in genetically susceptible mice.
title_full Fetal radiation exposure induces testicular cancer in genetically susceptible mice.
title_fullStr Fetal radiation exposure induces testicular cancer in genetically susceptible mice.
title_full_unstemmed Fetal radiation exposure induces testicular cancer in genetically susceptible mice.
title_sort fetal radiation exposure induces testicular cancer in genetically susceptible mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The prevalence of testicular germ cell tumors (TGCT), a common solid tissue malignancy in young men, has been annually increasing at an alarming rate of 3%. Since the majority of testicular cancers are derived from germ cells at the stage of transformation of primordial germ cell (PGC) into gonocytes, the increase has been attributed to maternal/fetal exposures to environmental factors. We examined the effects of an estrogen (diethylstilbestrol, DES), an antiandrogen (flutamide), or radiation on the incidence of testicular germ cell tumors in genetically predisposed 129.MOLF-L1 (L1) congenic mice by exposing them to these agents on days 10.5 and 11.5 of pregnancy. Neither flutamide nor DES produced noticeable increases in testis cancer incidence at 4 weeks of age. In contrast, two doses of 0.8-Gy radiation increased the incidence of TGCT from 45% to 100% in the offspring. The percentage of mice with bilateral tumors, weights of testes with TGCT, and the percentage of tumors that were clearly teratomas were higher in the irradiated mice than in controls, indicating that irradiation induced more aggressive tumors and/or more foci of initiation sites in each testis. This radiation dose did not disrupt spermatogenesis, which was qualitatively normal in tumor-free testes although they were reduced in size. This is the first proof of induction of testicular cancer by an environmental agent and suggests that the male fetus of women exposed to radiation at about 5-6 weeks of pregnancy might have an increased risk of developing testicular cancer. Furthermore, it provides a novel tool for studying the molecular and cellular events of testicular cancer pathogenesis.
url http://europepmc.org/articles/PMC3278464?pdf=render
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