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Key Role of CD151-integrin Complex in Lung Cancer Metastasis and Mechanisms Involved.
- Source :
-
Current medical science [Curr Med Sci] 2020 Dec; Vol. 40 (6), pp. 1148-1155. Date of Electronic Publication: 2021 Jan 11. - Publication Year :
- 2020
-
Abstract
- Tetraspanin CD151 was found to be upregulated in malignant cell types and has been identified as a tumor metastasis promoter. In this study, we aimed to examine the role of the CD151-integrin complex in lung cancer metastasis and the underlying mechanisms. CD151 QRD <superscript>194-196</superscript> →AAA <superscript>194-196</superscript> mutant was generated and used to transfect A549 human lung adenocarcinoma cells. We found that there was no significant difference in CD151 protein expression between CD151 and CD151-AAA mutant groups. In vitro, CD151-AAA mutant delivery abrogated the migration and invasion of A549 cells, which was promoted by CD151 gene transfer. Furthermore, CD151-AAA delivery failed to activate FAK and p130Cas signaling pathways. Western blot and immunohistochemical staining showed strong CD151 expression in lung cancerous tissues but not in adjacent normal tissues. Increased level of CD151 protein was observed in 20 of the patients and the positive rate of CD151 protein in specimens was 62.5% (20/32). In addition, CD151 was co-localized with α3 integrin at the cell-cell contact site in carcinoma tissues. These results suggested that the disruption of the CD151-α3 integrin complex may impair the metastasis-promoting effects and signaling events induced by CD151 in lung cancer. Our findings identified a key role for CD151-α3 integrin complex as a promoter in the lung cancer.
- Subjects :
- A549 Cells
Cell Movement
Crk-Associated Substrate Protein metabolism
Female
Focal Adhesion Kinase 1 metabolism
Humans
Lung Neoplasms genetics
Male
Mutation
Neoplasm Metastasis
Signal Transduction
Tetraspanin 24 genetics
Integrin alpha3 metabolism
Lung Neoplasms metabolism
Tetraspanin 24 metabolism
Up-Regulation
Subjects
Details
- Language :
- English
- ISSN :
- 2523-899X
- Volume :
- 40
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Current medical science
- Publication Type :
- Academic Journal
- Accession number :
- 33428143
- Full Text :
- https://doi.org/10.1007/s11596-020-2297-7