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Title: Poor recognition of O6-isopropyl dG by MGMT triggers double strand break-mediated cell death and micronucleus induction in FANC-deficient cells
Authors: Hashimoto, Kiyohiro
Sharma, Vyom
Sasanuma, Hiroyuki  kyouindb  KAKEN_id
Tian, Xu
Takata, Minoru  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-4926-3675 (unconfirmed)
Takeda, Shunichi
Swenberg, James A.
Nakamura, Jun
Author's alias: 笹沼, 博之
髙田, 穣
Keywords: Alkylation
DT40
FANC
Isopropyl methanesulfonate
Micronucleus
Issue Date: 29-Jul-2016
Publisher: Impact Journals LLC
Journal title: Oncotarget
Volume: 7
Issue: 37
Start page: 59795
End page: 59808
Abstract: Isopropyl methanesulfonate (IPMS) is the most potent genotoxic compound among methanesulfonic acid esters. The genotoxic potential of alkyl sulfonate esters is believed to be due to their alkylating ability of the O6 position of guanine. Understanding the primary repair pathway activated in response to IPMS-induced DNA damage is important to profile the genotoxic potential of IPMS. In the present study, both chicken DT40 and human TK6 cell-based DNA damage response (DDR) assays revealed that dysfunction of the FANC pathway resulted in higher sensitivity to IPMS compared to EMS or MMS. O6-alkyl dG is primarily repaired by methyl guanine methyltransferase (MGMT), while isopropyl dG is less likely to be a substrate for MGMT. Comparison of the cytotoxic potential of IPMS and its isomer n-propyl methanesulfonate (nPMS) revealed that the isopropyl moiety avoids recognition by MGMT and leads to higher cytotoxicity. Next, the micronucleus (MN) assay showed that FANC deficiency increases the sensitivity of DT40 cells to MN induction by IPMS. Pretreatment with O6-benzyl guanine (OBG), an inhibitor of MGMT, increased the MN frequency in DT40 cells treated with nPMS, but not IPMS. Lastly, IPMS induced more double strand breaks in FANC-deficient cells compared to wild-type cells in a time-dependent manner. All together, these results suggest that IPMS-derived O6- isopropyl dG escapes recognition by MGMT, and the unrepaired DNA damage leads to double strand breaks, resulting in MN induction. FANC, therefore, plays a pivotal role in preventing MN induction and cell death caused by IPMS.
Rights: All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
URI: http://hdl.handle.net/2433/218393
DOI(Published Version): 10.18632/oncotarget.10928
PubMed ID: 27486975
Appears in Collections:Journal Articles

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