PARPi increases radiotherapy sensitivity of esophageal squamous cell carcinoma by inhibiting XRCC1 expression

This study investigated the effect of poly-ADP ribose polymerase inhibitor (PARPi) on X-ray repair cross complementing 1 gene (XRCC1) expression and radiotherapy sensitivity of esophageal squamous cell carcinoma (ESCC). Tissue samples from patients with ESCC treated with irradiation using a linear a...

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Published inFu she yan jiu yu fu she gong yi xue bao Vol. 41; no. 3; p. 030303
Main Authors LI Yiping, ZHANG Yufei, SUN Guangzhi, YE Yunyao, SHEN Xiaozhou, HAN Gaohua
Format Journal Article
LanguageChinese
Published Science Press 01.06.2023
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Abstract This study investigated the effect of poly-ADP ribose polymerase inhibitor (PARPi) on X-ray repair cross complementing 1 gene (XRCC1) expression and radiotherapy sensitivity of esophageal squamous cell carcinoma (ESCC). Tissue samples from patients with ESCC treated with irradiation using a linear accelerator were collected to detect the expression of XRCC1 and PARP-1 with immunohistochemical staining, and the effect of their expression on radiotherapy efficacy was evaluated. A linear accelerator was used to irradiate ECA109 cells after treatment with different concentrations of AZD2281 (a PARP inhibitor) to detect the radiotherapy sensitization ratio (SER) of PARPi. An RT-PCR assay was used to assess the relative expression of XRCC1 mRNA in ECA109 cells treated with irradiation and AZD2281 and to explore the effect of PARPi on the transcription of the XRCC1 gene in ECA109 cells after irradiation. Our data indicated that the objective response rate (ORR) of XRCC1-positive patients was lower than that of XRCC1
AbstractList This study investigated the effect of poly-ADP ribose polymerase inhibitor (PARPi) on X-ray repair cross complementing 1 gene (XRCC1) expression and radiotherapy sensitivity of esophageal squamous cell carcinoma (ESCC). Tissue samples from patients with ESCC treated with irradiation using a linear accelerator were collected to detect the expression of XRCC1 and PARP-1 with immunohistochemical staining, and the effect of their expression on radiotherapy efficacy was evaluated. A linear accelerator was used to irradiate ECA109 cells after treatment with different concentrations of AZD2281 (a PARP inhibitor) to detect the radiotherapy sensitization ratio (SER) of PARPi. An RT-PCR assay was used to assess the relative expression of XRCC1 mRNA in ECA109 cells treated with irradiation and AZD2281 and to explore the effect of PARPi on the transcription of the XRCC1 gene in ECA109 cells after irradiation. Our data indicated that the objective response rate (ORR) of XRCC1-positive patients was lower than that of XRCC1
Author SHEN Xiaozhou
SUN Guangzhi
HAN Gaohua
ZHANG Yufei
LI Yiping
YE Yunyao
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  fullname: LI Yiping
  organization: Department of Oncology, Taizhou people’s Hospital affiliated to Nanjing Medical University, Taizhou 225300, China
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  fullname: ZHANG Yufei
  organization: Department of Oncology, Taizhou people’s Hospital affiliated to Nanjing Medical University, Taizhou 225300, China
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  fullname: SUN Guangzhi
  organization: Radiotherapy Center, Taizhou people’s Hospital affiliated to Nanjing Medical University, Taizhou 225300, China
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  fullname: YE Yunyao
  organization: Department of Oncology, Taizhou people’s Hospital affiliated to Nanjing Medical University, Taizhou 225300, China
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  fullname: SHEN Xiaozhou
  organization: Department of Oncology, Taizhou people’s Hospital affiliated to Nanjing Medical University, Taizhou 225300, China
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  fullname: HAN Gaohua
  organization: Department of Oncology, Taizhou people’s Hospital affiliated to Nanjing Medical University, Taizhou 225300, China
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Snippet This study investigated the effect of poly-ADP ribose polymerase inhibitor (PARPi) on X-ray repair cross complementing 1 gene (XRCC1) expression and...
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SubjectTerms esophageal squamous cell carcinoma
poly(adp-ribose)polymerase inhibitor
radiotherapy sensitivity
x-ray cross complementing gene-1
Title PARPi increases radiotherapy sensitivity of esophageal squamous cell carcinoma by inhibiting XRCC1 expression
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