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Targeting Neoantigens in Cancer: Possibilities and Opportunities in Breast Cancer
Zuhair Chaudhry1, Anik Boyadzhyan1, Kayvan Sasaninia1
1Department of Translational Research, College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, CA 91766, USA.
Abstract:
As one of the most prevalent forms of cancer worldwide, breast cancer has garnered significant attention within the clinical research setting. While traditional treatment employs a multidisciplinary approach including a variety of therapies such as chemotherapy, hormone therapy, and even surgery, researchers have since directed their attention to the budding role of neoantigens. Neoantigens are defined as tumor-specific antigens that result from a multitude of genetic alterations, the most prevalent of which is the single nucleotide variant. As a result of their foreign nature, neoantigens elicit immune responses upon presentation by Major Histocompatibility Complexes I and II followed by recognition by T cell receptors. Previously, researchers have been able to utilize these immunogenic properties and manufacture neoantigen-specific T-cells and neoantigen vaccines. Within the context of breast cancer, biomarkers such as tumor protein 53 (TP53), Survivin, Partner and Localizer of BRCA2 (PALB2), and protein tyrosine phosphatase receptor T (PTPRT) display exceeding potential to serve as neoantigens. However, despite their seemingly limitless potential, neoantigens must overcome various obstacles if they are to be fairly distributed to patients. For instance, a prolonged period between the identification of a neoantigen and the dispersal of treatment poses a serious risk within the context of breast cancer. Regardless of these current obstacles, it appears highly promising that future research into neoantigens will make an everlasting impact on the health outcomes within the realm of breast cancer. The purpose of this literature review is to comprehensively discuss the etiology of various forms of breast cancer and current treatment modalities followed by the significance of neoantigens in cancer therapeutics and their application to breast cancer. Further, we have discussed the limitations, future directions, and the role of transcriptomics in neoantigen identification and personalized medicine. The concepts discussed in the original and review articles were included in this review article.
Insights
Neoantigens, or tumor-specific antigens, show promise for treating breast cancer by eliciting immune responses. Future research into neoantigens could significantly improve patient outcomes despite current challenges in treatment delivery.
Area of Science:
- Oncology
- Immunology
- Genetics
Background:
- Breast cancer is a prevalent global cancer requiring diverse treatments.
- Neoantigens, arising from genetic alterations like single nucleotide variants, are tumor-specific and trigger immune responses.
- Biomarkers such as TP53, Survivin, PALB2, and PTPRT show potential as breast cancer neoantigens.
Purpose of the Study:
- To review breast cancer etiology and treatments.
- To discuss the significance and application of neoantigens in breast cancer therapeutics.
- To explore transcriptomics' role in neoantigen identification and personalized medicine.
Main Methods:
- Literature review synthesizing existing research on breast cancer and neoantigens.
- Analysis of neoantigen properties, including their immunogenicity and potential as biomarkers.
- Discussion of challenges and future directions in neoantigen-based cancer therapy.
Main Results:
- Neoantigens elicit T-cell mediated immune responses.
- Specific biomarkers (TP53, Survivin, PALB2, PTPRT) are identified as potential neoantigens in breast cancer.
- Current limitations include the time gap between neoantigen identification and treatment delivery.
Conclusions:
- Neoantigens hold significant promise for advancing breast cancer treatment.
- Overcoming delivery challenges is crucial for realizing the full potential of neoantigen therapies.
- Transcriptomics offers a pathway for personalized neoantigen identification and targeted therapies.
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