Journal of Cancer Immunology & Therapy

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Opinion Article - Journal of Cancer Immunology & Therapy (2023) Volume 6, Issue 4

Unveiling the Secrets of Immune Evasion in Tumor growth

Eric Chen *

Department of cancer

*Corresponding Author:
Eric Chen
Department of cancer
University of Manitoba
Canada
E-mail: echen2@cancercare.mb.ca

Received:31-Jul-2023,Manuscript No. AAJCIT-23-109867; Editor assigned: 04-Aug-2023, PreQC No. AAJCIT-23-109867 (PQ); Reviewed:18-Aug -2023, QC No. AAJCIT-23-109867; Revised:24-Aug -2023, Manuscript No. AAJCIT-23-109867 (R); Published:31-Aug -2023, DOI: 10.35841/aajcit- 6.4.165

Citation: Chen E. Unveiling the secrets of immune evasion in tumor growth. J Cancer Immunol Ther. 2023;6(4):165

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Abstract

  

Introduction

Cancer, one of the leading causes of death worldwide, has long been a formidable challenge in the field of medicine. Over the years, conventional treatments like chemotherapy, radiation, and surgery have made significant strides in combating cancer, but their limitations have prompted researchers to explore innovative approaches. Among these, immunotherapy has emerged as a promising frontier in cancer treatment, leveraging the power of the immune system to recognize and eliminate cancer cells. Understanding the complex interplay between cancer and the immune system is crucial for developing effective immunotherapeutic strategies. Cancer Immunology & Therapy, a burgeoning discipline within oncology, seeks to decipher the intricate mechanisms that govern the relationship between tumors and the immune system. Central to this investigation is the concept of immune evasion, whereby cancer cells employ a variety of tactics to evade detection and destruction by the immune system, thereby promoting tumor growth and metastasis. Unraveling these evasion mechanisms is paramount for devising targeted interventions that can bolster the immune response against cancer [1].

One of the primary ways in which cancer cells escape immune surveillance is through the modulation of immune checkpoints. Immune checkpoints are molecules on immune cells that can either activate or inhibit immune responses. They play a vital role in maintaining self-tolerance and preventing autoimmune reactions. However, cancer cells exploit these checkpoints, particularly programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), to dampen the immune response [2].

By binding to these checkpoints' ligands, cancer cells effectively shut down the immune cells' attack, making them virtually invisible to the immune system. Moreover, tumor cells often employ the tactic of downregulating major histocompatibility complex (MHC) molecules on their surfaces. MHC molecules play a crucial role in presenting antigens derived from cancer cells to the immune system. By reducing MHC expression, cancer cells impede the recognition of their abnormal features by immune cells, further thwarting an immune attack.Additionally, cancer cells can actively recruit suppressive immune cells, such as regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs), to create an immunosuppressive tumor microenvironment. These suppressive cells suppress effector T cells, which are responsible for recognizing and destroying cancer cells. As a result, the tumor microenvironment becomes a nurturing ground for cancer growth, fostering immune tolerance and allowing tumors to evade immune destruction [3]. 

Furthermore, cancer cells exhibit remarkable heterogeneity, leading to the emergence of tumor subclones with different antigenic profiles. This heterogeneity challenges the immune system's ability to target all cancer cells effectively, as therapies directed against a specific antigen may only impact a fraction of tumor cells, while others remain unscathed. The field of Cancer Immunology & Therapy offers a promising pathway towards overcoming the challenges posed by immune evasion in cancer. By comprehensively understanding the mechanisms underlying immune escape, researchers and clinicians can devise innovative strategies to reinvigorate the immune response against tumors. As ongoing research delves deeper into the intricate interactions between cancer and the immune system, the future of cancer treatment holds great promise, envisioning more effective and personalized therapies that harness the power of our own immune system to combat this devastating disease [4].

In the realm of cancer research, the burgeoning field of Cancer Immunology & Therapy has emerged as a beacon of hope in the quest for effective cancer treatments. Harnessing the power of the immune system to combat cancer cells, immunotherapy has shown remarkable success in certain cases. However, an ominous hurdle stands in the way of its full potential: immune evasion.Immune evasion is a cunning strategy employed by cancer cells to elude the immune system's surveillance and destruction mechanisms. Understanding the intricate mechanisms behind immune evasion is crucial for devising innovative and targeted therapies that can overcome resistance and significantly improve patient outcomes [5].

 

References

  1. Giraldo NA, Becht E, Remark R, et al The immune contexture of primary and metastatic human tumours Curr Opin Immunol. 2014;27:8-15.
  2. Indexed at, Google Scholar, Cross Ref

  3. Snyder A, Chan TA.Immunogenic peptide discovery in cancer genomes.. Curr Opin Genet Dev. 2015;30:7-16.
  4. Indexed at, Google ScholarCross Ref

  5. Mlecnik B, Tosolini M, Kirilovsky A, et al . Histopathologic-based prognostic factors of colorectal cancers are associated with the state of the local immune reaction. J Clin Oncol. 2011;29(6):610-8.
  6. Indexed at, Google Scholar, Cross Ref

  7. Britten CM, Janetzki S, Van der Burg SH, et al.Minimal information about T cell assays: The process of reaching the community of T cell immunologists in cancer and beyond. Cancer Immunol Immunother. 2011;60:15-22.

    Indexed atGoogle Scholar, Cross Ref

  8. Groth C, Hu X, Weber R, et al.. Immunosuppression mediated by myeloid-derived suppressor cells (MDSCs) during tumour progression Br J Cancer. 2019;120(1):16-25.
  9. Indexed at, Google Scholar, Cross Ref

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