Updated Clinical Perspectives and Challenges of Chimeric Antigen Receptor-T Cell Therapy in Colorectal Cancer and Invasive Breast Cancer
- PMID: 37566162
- DOI: 10.1007/s00005-023-00684-x
Updated Clinical Perspectives and Challenges of Chimeric Antigen Receptor-T Cell Therapy in Colorectal Cancer and Invasive Breast Cancer
Abstract
In recent years, the incidence of colorectal cancer (CRC) and breast cancer (BC) has increased worldwide and caused a higher mortality rate due to the lack of selective anti-tumor therapies. Current chemotherapies and surgical interventions are significantly preferred modalities to treat CRC or BC in advanced stages but the prognosis for patients with advanced CRC and BC remains dismal. The immunotherapy technique of chimeric antigen receptor (CAR)-T cells has resulted in significant clinical outcomes when treating hematologic malignancies. The novel CAR-T therapy target antigens include GUCY2C, CLEC14A, CD26, TEM8/ANTXR1, PDPN, PTK7, PODXL, CD44, CD19, CD20, CD22, BCMA, GD2, Mesothelin, TAG-72, CEA, EGFR, B7H3, HER2, IL13Ra2, MUC1, EpCAM, PSMA, PSCA, NKG2D. The significant aim of this review is to explore the recently updated information pertinent to several novel targets of CAR-T for CRC, and BC. We vividly described the challenges of CAR-T therapies when treating CRC or BC. The immunosuppressive microenvironment of solid tumors, the shortage of tumor-specific antigens, and post-treatment side effects are the major hindrances to promoting the development of CAR-T cells. Several clinical trials related to CAR-T immunotherapy against CRC or BC have already been in progress. This review benefits academicians, clinicians, and clinical oncologists to explore more about the novel CAR-T targets and overcome the challenges during this therapy.
Keywords: Breast cancer; CAR-T; Challenges; Colorectal cancer; Immunotherapy; Novel CAR-T targets; Solid tumor.
© 2023. L. Hirszfeld Institute of Immunology and Experimental Therapy, Wroclaw, Poland.
Similar articles
-
Cell Therapy for Colorectal Cancer: The Promise of Chimeric Antigen Receptor (CAR)-T Cells.Int J Mol Sci. 2021 Oct 29;22(21):11781. doi: 10.3390/ijms222111781. Int J Mol Sci. 2021. PMID: 34769211 Free PMC article. Review.
-
[Advances of CAR-T cell therapy in treating colorectal cancer].Sheng Wu Gong Cheng Xue Bao. 2024 May 25;40(5):1365-1379. doi: 10.13345/j.cjb.230741. Sheng Wu Gong Cheng Xue Bao. 2024. PMID: 38783803 Review. Chinese.
-
Challenges of chimeric antigen receptor-T/natural killer cell therapy in the treatment of solid tumors: focus on colorectal cancer and evaluation of combination therapies.Mol Cell Biochem. 2023 May;478(5):967-980. doi: 10.1007/s11010-022-04568-0. Epub 2022 Oct 3. Mol Cell Biochem. 2023. PMID: 36190614 Review.
-
Chimeric antigen receptor-based immunotherapy in breast cancer: Recent progress in China.Cancer. 2024 Apr 15;130(S8):1378-1391. doi: 10.1002/cncr.35096. Epub 2023 Nov 11. Cancer. 2024. PMID: 37950749 Review.
-
The landscape of chimeric antigen receptor T cell therapy in breast cancer: Perspectives and outlook.Front Immunol. 2022 Jul 22;13:887471. doi: 10.3389/fimmu.2022.887471. eCollection 2022. Front Immunol. 2022. PMID: 35935930 Free PMC article. Review.
Cited by
-
Inhibition of Pard3 promotes breast cancer metastasis via the USP28 mediated deubiquitination of Snail1.Heliyon. 2023 Nov 20;9(12):e22599. doi: 10.1016/j.heliyon.2023.e22599. eCollection 2023 Dec. Heliyon. 2023. PMID: 38076191 Free PMC article.
-
A comparative in vitro study on the effect of SGLT2 inhibitors on chemosensitivity to doxorubicin in MCF-7 breast cancer cells.Oncol Res. 2024 Apr 23;32(5):817-830. doi: 10.32604/or.2024.048988. eCollection 2024. Oncol Res. 2024. PMID: 38686050 Free PMC article.
-
Exploring the relationship between anastasis and mitochondrial ROS-mediated ferroptosis in metastatic chemoresistant cancers: a call for investigation.Front Immunol. 2024 Jul 2;15:1428920. doi: 10.3389/fimmu.2024.1428920. eCollection 2024. Front Immunol. 2024. PMID: 39015566 Free PMC article. Review.
-
Clinical research progress of callisperes® of drug-loaded microsphere arterial chemoembolisation in the treatment of solid tumors.Discov Oncol. 2024 May 13;15(1):161. doi: 10.1007/s12672-024-01030-z. Discov Oncol. 2024. PMID: 38739205 Free PMC article. Review.
-
Recent advances in CAR-T cell therapy for acute myeloid leukaemia.J Cell Mol Med. 2024 May;28(9):e18369. doi: 10.1111/jcmm.18369. J Cell Mol Med. 2024. PMID: 38712978 Free PMC article. Review.
References
-
- Ahn JC, Teng PC, Chen PJ et al (2021) Detection of circulating tumor cells and their implications as a biomarker for diagnosis, prognostication, and therapeutic monitoring in hepatocellular carcinoma. Hepatology 73:422–436. https://doi.org/10.1002/hep.31165 - DOI - PubMed
-
- Amatya C, Pegues MA, Lam N et al (2021) Development of CAR T cells expressing a suicide gene plus a chimeric antigen receptor targeting signaling lymphocytic-activation molecule F7. Mol Ther 29:702–717. https://doi.org/10.1016/j.ymthe.2020.10.008 - DOI - PubMed
-
- Aoe T, Goto S, Ohno H et al (1994) Different cytoplasmic structure of the CD3ζ family dimer modulates the activation signal and function of T cells. Int Immunol 6:1671–1679. https://doi.org/10.1093/intimm/6.11.1671 - DOI - PubMed
-
- Baybutt T, Snook A, Waldman S et al (2020) 105 A third-generation human GUCY2C-targeted CAR-T cell for colorectal cancer immunotherapy. J Immunother Cancer 8(Suppl 3):A116–A116. https://doi.org/10.1136/jitc-2020-SITC2020.0105 - DOI
-
- Boice M, Salloum D, Mourcin F et al (2016) Loss of the HVEM tumor suppressor in lymphoma and restoration by modified CAR-T cells. Cell 167:405–418. https://doi.org/10.1016/j.cell.2016.08.032 - DOI - PubMed - PMC
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous