1. Academic Validation
  2. Altered polymerase theta expression promotes chromosomal instability in salivary adenoid cystic carcinoma

Altered polymerase theta expression promotes chromosomal instability in salivary adenoid cystic carcinoma

  • J Cell Mol Med. 2022 Jul;26(14):3931-3949. doi: 10.1111/jcmm.17429.
Han Bai 1 Shilin Xia 2 Lei Zhu 1 Yan Dong 1 Chao Liu 1 Nan Li 1 3 Han Liu 1 3 Jing Xiao 1 3
Affiliations

Affiliations

  • 1 College of Stomatology, Dalian Medical University, Dalian, China.
  • 2 Clinical Laboratory of Integrative Medicine, The First Affiliated Hospital of Dalian Medical University, Dalian, China.
  • 3 Liaoning Province Key Laboratory of Organism Microecology and Disease Control, Dalian, China.
Abstract

Genomic instability (GIN) plays a key role in Cancer progression. The disorders of polymerase theta (POLQ) were reported to contribute to GIN and progression in many cancers. Here, we found that POLQ over-expression was related to salivary adenoid cystic carcinoma (SACC) progression and poor prognosis. Then, we investigated the role and mechanism of POLQ in the GIN in SACC. GIN was assessed by chromosome staining with DAPI and Giemsa, as well as qRT-PCR of the mitosis-related gene expression. Meanwhile, PCR-SSCP was used to evaluate microsatellite instability. Modulation of POLQ expression increased chromosomal instability and enhanced the sensitivity to etoposide without impacting microsatellite stability. Mechanistically, POLQ regulated genome stability by promoting the expression of the error-prone alt-NHEJ-related protein PARP1, and down-regulating c-NHEJ- and HR-related proteins KU70 and RAD51. In vitro CCK, Transwell assays and in vivo murine xenograft models indicated that the PARP Inhibitor olaparib suppressed SACC growth in the case of etoposide-induced DNA damage. Bioinformatic analysis identified CEBPB as a potential POLQ-regulating transcription factor. In summary, our research provides new insights into the mechanisms of SACC chromosomal instability and identifies new potential targets for SACC treatment.

Keywords

CEBPB; DNA repair; POLQ; SACC; chromosomal instability.

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