4.6 Review

Tumor Heterogeneity: A Great Barrier in the Age of Cancer Immunotherapy

期刊

CANCERS
卷 13, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13040806

关键词

tumor heterogeneity; antigen escape; immunotherapy; cancer

类别

资金

  1. Canadian Cancer Society Research Institute
  2. Canadian Institutes for Health Research
  3. Terry Fox Research Institute
  4. Vanier Canada Graduate Scholarship

向作者/读者索取更多资源

Tumor heterogeneity remains a major obstacle in successful cancer treatment, arising from changes in the tumor microenvironment and leading to the presence of different malignant subpopulations within a single tumor mass. Therapeutic interventions can increase selective pressure towards resistant subpopulations, often causing relapse in previously responsive patients. Strategies such as multi-therapy regimens are being employed to combat intrinsic resistance mechanisms, especially in the field of cancer immunotherapy, where antigen escape and immunosuppression are common forms of acquired resistance.
Simple Summary Despite great advances in cancer therapy, tumor heterogeneity continues to be a great barrier for the successful treatment of cancer. It has long been established that tumor heterogeneity is prevelant in most cancer patients and is a major driver of acquired resistance to all forms of cancer therapy. In the case of immunotherapy, the response of the immune system against specific tumor antigens can drive selective pressure towards antigen-negative cells, which is a common cause of relapse in the clinic. In this review we summarize the mechanisms in which tumor heterogeity can arise. Furthermore, we discuss recent advances in the field of oncology that can be used to better identify, study, and overcome tumor heterogeneity. Throughout the history of oncology research, tumor heterogeneity has been a major hurdle for the successful treatment of cancer. As a result of aberrant changes in the tumor microenvironment such as high mutational burden, hypoxic conditions and abnormal vasculature, several malignant subpopulations often exist within a single tumor mass. Therapeutic intervention can also increase selective pressure towards subpopulations with acquired resistance. This phenomenon is often the cause of relapse in previously responsive patients, drastically changing the expected outcome of therapy. In the case of cancer immunotherapy, tumor heterogeneity is a substantial barrier as acquired resistance often takes the form of antigen escape and immunosuppression. In an effort to combat intrinsic resistance mechanisms, therapies are often combined as a multi-pronged approach to target multiple pathways simultaneously. These multi-therapy regimens have long been a mainstay of clinical oncology with chemotherapy cocktails but are more recently being investigated in the emerging landscape of immunotherapy. Furthermore, as high throughput technology becomes more affordable and accessible, researchers continue to deepen their understanding of the factors that influence tumor heterogeneity and shape the TME over the course of treatment regimens. In this review, we will investigate the factors that give rise to tumor heterogeneity and the impact it has on the field of immunotherapy. We will discuss how tumor heterogeneity causes resistance to various treatments and review the strategies currently being employed to overcome this challenging clinical hurdle. Finally, we will outline areas of research that should be prioritized to gain a better understanding of tumor heterogeneity and develop appropriate solutions.

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