PIM1/STAT3 axis: a potential co-targeted therapeutic approach in triple-negative breast cancer
- PMID: 35568774
- DOI: 10.1007/s12032-022-01675-2
PIM1/STAT3 axis: a potential co-targeted therapeutic approach in triple-negative breast cancer
Abstract
Triple-negative breast cancer lacks an expression of ER, PR, and Her-2, has a poor prognosis, and there are no target therapies available. Therapeutic options to treat TNBC are limited and urgently needed. Strong evidence indicates that molecular signaling pathways have a significant function to regulate biological mechanisms and their abnormal expression endows with the development of cancer. PIM kinase is overexpressed in various human cancers including TNBC which is regulated by various signaling pathways that are crucial for cancer cell proliferation and survival and also make PIM kinase as an attractive drug target. One of the targets of the STAT3 signaling pathway is PIM1 that plays a key role in tumor progression and transformation. In this review, we accumulate the current scenario of the PIM-STAT3 axis that provides insights into the PIM1 and STAT3 inhibitors which can be developed as potential co-inhibitors as prospective anticancer agents.
Keywords: PIM inhibitors; PIM1; STAT3; STAT3 inhibitors; Triple-negative breast cancer.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Similar articles
-
Neoprzewaquinone A Inhibits Breast Cancer Cell Migration and Promotes Smooth Muscle Relaxation by Targeting PIM1 to Block ROCK2/STAT3 Pathway.Int J Mol Sci. 2023 Mar 13;24(6):5464. doi: 10.3390/ijms24065464. Int J Mol Sci. 2023. PMID: 36982538 Free PMC article.
-
STAT3 as a potential therapeutic target in triple negative breast cancer: a systematic review.J Exp Clin Cancer Res. 2019 May 14;38(1):195. doi: 10.1186/s13046-019-1206-z. J Exp Clin Cancer Res. 2019. PMID: 31088482 Free PMC article.
-
PIM1 kinase inhibition as a targeted therapy against triple-negative breast tumors with elevated MYC expression.Nat Med. 2016 Nov;22(11):1321-1329. doi: 10.1038/nm.4213. Epub 2016 Oct 24. Nat Med. 2016. PMID: 27775705 Free PMC article.
-
PIM1 kinase regulates cell death, tumor growth and chemotherapy response in triple-negative breast cancer.Nat Med. 2016 Nov;22(11):1303-1313. doi: 10.1038/nm.4198. Epub 2016 Oct 24. Nat Med. 2016. PMID: 27775704 Free PMC article.
-
PIM1: a promising target in patients with triple-negative breast cancer.Med Oncol. 2017 Aug;34(8):142. doi: 10.1007/s12032-017-0998-y. Epub 2017 Jul 18. Med Oncol. 2017. PMID: 28721678 Review.
Cited by
-
PIM1 kinase and its diverse substrate in solid tumors.Cell Commun Signal. 2024 Nov 1;22(1):529. doi: 10.1186/s12964-024-01898-y. Cell Commun Signal. 2024. PMID: 39487435 Free PMC article. Review.
-
Unravelling the potency of the 4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile scaffold with S-arylamide hybrids as PIM-1 kinase inhibitors: synthesis, biological activity and in silico studies.RSC Med Chem. 2025 Mar 28. doi: 10.1039/d5md00021a. Online ahead of print. RSC Med Chem. 2025. PMID: 40162200 Free PMC article.
-
Targeting Stem Cells and Dysplastic Features With Dual MEK/ERK and STAT3 Suppression in Gastric Carcinogenesis.Gastroenterology. 2024 Jan;166(1):117-131. doi: 10.1053/j.gastro.2023.09.040. Epub 2023 Oct 4. Gastroenterology. 2024. PMID: 37802423 Free PMC article.
-
Physcion increases the sensitivity of hepatocellular carcinoma to sorafenib through miRNA-370/PIM1 axis-regulated glycolysis.World J Gastrointest Oncol. 2023 Aug 15;15(8):1400-1411. doi: 10.4251/wjgo.v15.i8.1400. World J Gastrointest Oncol. 2023. PMID: 37663938 Free PMC article.
-
Silencing PIM1 inhibits ENO1-induced AKT activation and attenuates fibrillogenesis during spinal cord injury-induced skeletal muscle atrophy.J Biol Chem. 2025 Jun 19;301(8):110398. doi: 10.1016/j.jbc.2025.110398. Online ahead of print. J Biol Chem. 2025. PMID: 40543593 Free PMC article.
References
-
- Lehmann BD, Pietenpol JA. Clinical implications of molecular heterogeneity in triple negative breast cancer. Breast. 2015;24(Suppl 2):S36-40. - PubMed
-
- Bayraktar S, Gluck S. Molecularly targeted therapies for metastatic triple-negative breast cancer. Breast Cancer Res Treat. 2013;138(1):21–35. - PubMed
-
- Nath A, et al. Molecular targets and therapeutics in chemoresistance of triple-negative breast cancer. Med Oncol. 2021;39(1):14. - PubMed
-
- Cuypers HT, et al. Murine leukemia virus-induced T-cell lymphomagenesis: integration of proviruses in a distinct chromosomal region. Cell. 1984;37(1):141–50. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous