JAK2 regulates paclitaxel resistance in triple negative breast cancers
- PMID: 34626199
- DOI: 10.1007/s00109-021-02138-3
JAK2 regulates paclitaxel resistance in triple negative breast cancers
Abstract
We investigated the molecular mechanisms of paclitaxel resistance in TNBC using seven patient-derived xenograft (PDX) models and TNBC cell lines. Among the seven PDX models, four models showed resistance to paclitaxel. Dysregulation of JAK/STAT pathways and JAK2 copy number gains were observed in the four paclitaxel-resistant PDX tumors. In TNBC cell lines, silencing the JAK2 gene showed a significant but mild synergistic effect when combined with paclitaxel in vitro. However, JAK1/2 inhibitor treatment resulted in restoration of paclitaxel sensitivity in two out of four paclitaxel-resistant PDX models and JAK1/2 inhibitor alone significantly suppressed the tumor growth in one out of the two remaining PDX models. Transcriptome data derived from the murine microenvironmental cells revealed an enrichment of genes involved in the cell cycle processes among the four paclitaxel-resistant PDX tumors. Histologic examination of those PDX tumor tissues showed increased Ki67-positive fibroblasts in the tumor microenvironment. Among the four different cancer-associated fibroblast (CAF) subtypes, cycling CAF exhibiting features of active cell cycle was enriched in the paclitaxel-resistant PDX tumors. Additionally, fibroblasts treated with the conditioned media from the JAK2-silenced breast cancer cells showed downregulation of cell cycle-related genes. Our data suggest that the JAK2 gene may play a critical role in determining responses of TNBC to paclitaxel by modulating the intrinsic susceptibility of cancer cells against paclitaxel and also by eliciting functional transitions of CAF subtypes in the tumor microenvironment. KEY MESSAGES : We investigated the molecular mechanisms of paclitaxel resistance in TNBC. JAK2 signaling was associated with paclitaxel resistance in TNBC PDX models. Paclitaxel-resistant PDX tumors were enriched with microenvironment cCAF subpopulation. JAK2 regulated paclitaxel-resistant CAF phenotype transition.
Keywords: Breast cancer; Fibroblast; JAK2; Microenvironment; Paclitaxel; Triple negative breast cancer.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Similar articles
-
BRCA1-IRIS inactivation overcomes paclitaxel resistance in triple negative breast cancers.Breast Cancer Res. 2015 Jan 13;17(1):5. doi: 10.1186/s13058-014-0512-9. Breast Cancer Res. 2015. PMID: 25583261 Free PMC article.
-
Combined inhibition of JAK2-STAT3 and SMO-GLI1/tGLI1 pathways suppresses breast cancer stem cells, tumor growth, and metastasis.Oncogene. 2020 Oct;39(42):6589-6605. doi: 10.1038/s41388-020-01454-1. Epub 2020 Sep 14. Oncogene. 2020. PMID: 32929154 Free PMC article.
-
Truncated HDAC9 identified by integrated genome-wide screen as the key modulator for paclitaxel resistance in triple-negative breast cancer.Theranostics. 2020 Sep 2;10(24):11092-11109. doi: 10.7150/thno.44997. eCollection 2020. Theranostics. 2020. PMID: 33042272 Free PMC article.
-
LncRNAs in modulating cancer cell resistance to paclitaxel (PTX) therapy.Med Oncol. 2024 Dec 13;42(1):28. doi: 10.1007/s12032-024-02577-1. Med Oncol. 2024. PMID: 39671022 Review.
-
Paclitaxel resistance in breast cancer: Current challenges and recent advanced therapeutic strategies.Cancer Treat Res Commun. 2025;43:100918. doi: 10.1016/j.ctarc.2025.100918. Epub 2025 Mar 31. Cancer Treat Res Commun. 2025. PMID: 40215760 Review.
Cited by
-
Potential Perturbations of Critical Cancer-regulatory Genes in Triple-Negative Breast Cancer Cells Within the Humanized Microenvironment of Patient-derived Xenograft Models.J Breast Cancer. 2024 Feb;27(1):37-53. doi: 10.4048/jbc.2023.0177. Epub 2024 Jan 15. J Breast Cancer. 2024. PMID: 38233337 Free PMC article.
-
AKR1C2 Promotes Metastasis and Regulates the Molecular Features of Luminal Androgen Receptor Subtype in Triple Negative Breast Cancer Cells.J Breast Cancer. 2023 Feb;26(1):60-76. doi: 10.4048/jbc.2023.26.e1. Epub 2022 Dec 16. J Breast Cancer. 2023. PMID: 36762781 Free PMC article.
-
Hypoxia-induced paclitaxel resistance in cervical cancer modulated by miR-100 targeting of USP15.Gynecol Oncol Rep. 2023 Jan 21;45:101138. doi: 10.1016/j.gore.2023.101138. eCollection 2023 Feb. Gynecol Oncol Rep. 2023. PMID: 36714373 Free PMC article.
-
A tubulin binding molecule drives differentiation of acute myeloid leukemia cells.iScience. 2022 Jul 19;25(8):104787. doi: 10.1016/j.isci.2022.104787. eCollection 2022 Aug 19. iScience. 2022. PMID: 35992086 Free PMC article.
-
Hypoxia: syndicating triple negative breast cancer against various therapeutic regimens.Front Oncol. 2023 Jul 10;13:1199105. doi: 10.3389/fonc.2023.1199105. eCollection 2023. Front Oncol. 2023. PMID: 37492478 Free PMC article. Review.
References
-
- Jung KW, Won YJ, Kong HJ, Lee ES (2018) Community of population-based regional cancer R. Cancer Statistics in Korea: Incidence, Mortality, Survival, and Prevalence in 2015. Cancer Res Treat 50(2):303–16
-
- Han J, Lee HB, Lee ES, Kang YJ, Kim Y, Choi J et al (2017) The treatment outcomes and the use of adjuvant therapies in breast cancer patients with severe co-morbidities. PLoS One 12(3):e0173721
-
- Holohan C, Van Schaeybroeck S, Longley DB, Johnston PG (2013) Cancer drug resistance: an evolving paradigm. Nat Rev Cancer 13(10):714–726 - PubMed
-
- Citron ML, Berry DA, Cirrincione C, Hudis C, Winer EP, Gradishar WJ et al (2003) Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: first report of Intergroup Trial C9741/Cancer and Leukemia Group B Trial 9741. J Clin Oncol 21(8):1431–1439 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous