Literature DB >> 31642059

Single peptides and combination modalities for triple negative breast cancer.

Atefeh Razazan1,2, Javad Behravan1,3,4.   

Abstract

Unlike other types of breast cancers (BCs), no specific therapeutic targets have been established for triple negative breast cancer (TNBC). Therefore, chemotherapy and radiotherapy are the only available adjuvant therapeutic choices for TNBC. New emerging reports show that TNBC is associated with higher numbers of intratumoral tumor infiltrating lymphocytes. This is indicative of host anti-TNBC immune surveillance and suggesting that immunotherapy can be considered as a therapeutic approach for TNBC management. Recent progress in molecular mechanisms of tumor-immune system interaction and cancer vaccine development studies, fast discoveries and FDA approvals of immune checkpoint inhibitors, chimeric antigen receptor T-cells, and oncolytic virotherapy have significantly attracted attention and research directions toward the immunotherapeutic approach to TNBC. Here in this review different aspects of TNBC immunotherapies including the host immune system-tumor interactions, the tumor microenvironment, the relevant molecular targets for immunotherapy, and clinical trials in the field are discussed.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  Immune checkpoint inhibitors; Triple negative breast cancer; Vaccines

Mesh:

Substances:

Year:  2019        PMID: 31642059     DOI: 10.1002/jcp.29300

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  2 in total

Review 1.  The Characteristics of Tumor Microenvironment in Triple Negative Breast Cancer.

Authors:  Yiqi Fan; Shuai He
Journal:  Cancer Manag Res       Date:  2022-01-03       Impact factor: 3.989

Review 2.  Extracellular Vesicles: The Landscape in the Progression, Diagnosis, and Treatment of Triple-Negative Breast Cancer.

Authors:  Menglu Dong; Quan Liu; Yi Xu; Qi Zhang
Journal:  Front Cell Dev Biol       Date:  2022-03-01
  2 in total

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