Effects of free fatty acid receptor (FFAR) signaling on the modulation of cancer cell functions under hypoxic conditions
In the tumor environment, hypoxia promotes tumor progression, such as cancer cell growth, migration and chemoresistance. This study aimed to evaluate the roles of free fatty acid receptors (FFARs) in the regulation of cancer cell functions under hypoxic conditions, using fibrosarcoma HT1080 cells. H...
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Veröffentlicht in: | Biochemical and biophysical research communications 2024-03, Vol.699, p.149554, Article 149554 |
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Zusammenfassung: | In the tumor environment, hypoxia promotes tumor progression, such as cancer cell growth, migration and chemoresistance. This study aimed to evaluate the roles of free fatty acid receptors (FFARs) in the regulation of cancer cell functions under hypoxic conditions, using fibrosarcoma HT1080 cells. HT1080 cells expressed FFAR1, FFAR2 and FFAR3 genes, but not FFAR4 gene. FFAR1, FFAR2 and FFAR3 expression levels in HT1080 cells cultured at 1 % O2 were elevated, compared with 21 % O2. The cell growth activities of HT1080 cells cultured at 21 % O2 were inhibited by acetic acid (AA) and propanoic acid (PA), but not 1 % O2. HT1080 cell motility was markedly reduced by culturing at 1 % O2. The cell growth and motility of HT1080 cells were enhanced by FFAR2 knockdown. The cell viability to cisplatin (CDDP) of HT1080 cells cultured at 1 % O2 was increased, compared with 21 % O2. FFAR2 knockdown suppressed the cell viability to CDDP of HT1080 cells. On the other hand, the cell motility and viability to CDDP of HT1080 cells cultured at 21 % O2 were suppressed by TUG-770. When HT1080 cells were cultured at 1 % O2, the cell motility and viability to CDDP were decreased, correlating with FFAR1 expression level. Moreover, FFAR1 knockdown increased the cell viability to CDDP of HT1080 cells cultured at 1 % O2. These results suggest that FFAR-mediated signaling plays an important role in the modulation of cellular functions of HT1080 cells under hypoxic conditions.
•FFAR1, FFAR2 and FFAR3 expressions in HT1080 cells were elevated by culturing at 1 % O2.•FFAR2 inhibited and FFAR3 stimulated cell growth and migration of HT1080 cells cultured at 1 % O2.•Cell viability to CDDP was enhanced by Gi protein via FFAR2 and FFAR3 in HT1080 cells cultured at 1 % O2.•HT1080 cell motility and viability to CDDP at 1 % O2 were suppressed by FFAR1.•FFARs are involved in the modulation of cellular functions of HT1080 cells under hypoxic conditions. |
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ISSN: | 0006-291X 1090-2104 1090-2104 |
DOI: | 10.1016/j.bbrc.2024.149554 |