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Influence of GPRC5A-Regulated ABCB1 Expression on Lung Adenocarcinoma Proliferation.
Li, Yun; Cui, Wen-Wen; Yang, Zhong-Fa; Liu, Wen-Hao; Bian, Mao-Wang; Deng, Jiong; Wang, Tong.
Afiliação
  • Li Y; Department of Physiology, School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261021, Shandong, China.
  • Cui WW; Department of Physiology, School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261021, Shandong, China.
  • Yang ZF; Department of Physiology, School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261021, Shandong, China.
  • Liu WH; Department of Physiology, School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261021, Shandong, China.
  • Bian MW; Department of Physiology, School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261021, Shandong, China.
  • Deng J; Medical Research Center, Affiliated Hospital of Binzhou Medical University, Binzhou 256600, Shandong, China.
  • Wang T; Department of Physiology, School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261021, Shandong, China.
Chin Med Sci J ; 39(1): 9-18, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38426412
ABSTRACT
Objective Aberrant expression of ATP binding cassette subfamily B member 1 (ABCB1) plays a key role in several cancers. However, influence of G protein coupled receptor family C group 5 type A (GPRC5A)-regulated ABCB1 expression on lung adenocarcinoma proliferation remains unclear. Therefore, this study investigated the effect of GPRC5A regulated ABCB1 expression on the proliferation of lung adenocarcinoma. Methods ABCB1 expressions in lung adenocarcinoma cell lines, human lung adenocarcinoma tissues, and tracheal epithelial cells and lung tissues of GPRC5A knockout mice and wild-type mice were analyzed with RT-PCR, Western blot, or immunohistochemical analysis. Cell counting kit-8 assay was performed to analyze the sensitivity of tracheal epithelial cells from GPRC5A knockout mice to chemotherapeutic agents. Subcutaneous tumor formation assay was performed to confirm whether down-regulation of ABCB1 could inhibit the proliferation of lung adenocarcinoma in vivo. To verify the potential regulatory relationship between GPRC5A and ABCB1, immunofluorescence and immunoprecipitation assays were performed. Results ABCB1 expression was up-regulated in lung adenocarcinoma cell lines and human lung adenocarcinoma tissues. ABCB1 expression in the tracheal epithelial cells and lung tissues of GPRC5Adeficient mice was higher than that in the wild type mice. Tracheal epithelial cells of GPRC5A knockout mice were much more sensitive to tariquidar and doxorubicin than those of GPRC5A wild type mice. Accordingly, 28 days after injection of the transplanted cells, the volume and weight of lung tumor in ABCB1knockout cell-transplanted GPRC5A-/-C57BL/6 mice were significantly smaller than those in wild type cell-transplanted mice (P= 0.0043, P= 0.0060). Furthermore, immunofluorescence and immunoprecipitation assays showed that GPRC5A regulated ABCB1 expression by direct binding.Conclusion GPRC5A reduces lung adenocarcinoma proliferation via inhibiting ABCB1 expression. The pathway by which GPRC5A regulates ABCB1 expression needs to be investigated.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adenocarcinoma de Pulmão / Neoplasias Pulmonares Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adenocarcinoma de Pulmão / Neoplasias Pulmonares Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article