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Pharmacological attenuation of melanoma by tryptanthrin pertains to the suppression of MITF-M through MEK/ERK signaling axis.
- Source :
-
Cellular and molecular life sciences : CMLS [Cell Mol Life Sci] 2022 Aug 10; Vol. 79 (9), pp. 478. Date of Electronic Publication: 2022 Aug 10. - Publication Year :
- 2022
-
Abstract
- Melanoma is the most aggressive among all types of skin cancers. The current strategies against melanoma utilize BRAF <superscript>V600E</superscript> , as a focal point for targeted therapy. However, therapy resistance developed in melanoma patients against the conventional anti-melanoma drugs hinders the ultimate benefits of targeted therapies. A major mechanism by which melanoma cells attain therapy resistance is via the activation of microphthalmia-associated transcription factor-M (MITF-M), the key transcription factor and oncogene aiding the survival of melanoma cells. We demonstrate that tryptanthrin (Tpn), an indole quinazoline alkaloid, which we isolated and characterized from Wrightia tinctoria, exhibits remarkable anti-tumor activity towards human melanoma through the down-regulation of MITF-M. Microarray analysis of Tpn-treated melanoma cells followed by a STRING protein association network analysis revealed that differential expression of genes in melanoma converges at MITF-M. Furthermore, in vitro and in vivo studies conducted using melanoma cells with differential MITF-M expression status, endogenously or ectopically, demonstrated that the anti-melanoma activity of Tpn is decisively contingent on its efficacy in down-regulating MITF-M expression. Tpn potentiates the degradation of MITF-M via the modulation of MEK1/2-ERK1/2-MITF-M signaling cascades. Murine models demonstrate the efficacy of Tpn in attenuating the migration and metastasis of melanoma cells, while remaining pharmacologically safe. In addition, Tpn suppresses the expression of mutated BRAF <superscript>V600E</superscript> and inhibits Casein Kinase 2α, a pro-survival enzyme that regulates ERK1/2 homeostasis in many tumor types, including melanoma. Together, we point to a promising anti-melanoma drug in Tpn, by virtue of its attributes to impede melanoma invasion and metastasis by attenuating MITF-M.<br /> (© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)
- Subjects :
- Animals
Cell Line, Tumor
Cell Proliferation
Gene Expression Regulation, Neoplastic
Humans
MAP Kinase Signaling System
Mice
Mitogen-Activated Protein Kinase Kinases metabolism
Proto-Oncogene Proteins B-raf genetics
Proto-Oncogene Proteins B-raf metabolism
Quinazolines
Melanoma genetics
Microphthalmia-Associated Transcription Factor genetics
Microphthalmia-Associated Transcription Factor metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1420-9071
- Volume :
- 79
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Cellular and molecular life sciences : CMLS
- Publication Type :
- Academic Journal
- Accession number :
- 35948813
- Full Text :
- https://doi.org/10.1007/s00018-022-04476-y