Small Molecule Targeting Immune Cells: A Novel Approach for Cancer Treatment

Conventional and cancer immunotherapies encompass diverse strategies to address various cancer types and stages. However, combining these approaches often encounters limitations such as non-specific targeting, resistance development, and high toxicity, leading to suboptimal outcomes in many cancers....

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Main Authors: Shilpi Singh, Debashis Barik, Ananta Prasad Arukha, Sujata Prasad, Iteeshree Mohapatra, Amar Singh, Gatikrushna Singh
Format: Article
Language:English
Published: MDPI AG 2023-09-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/11/10/2621
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author Shilpi Singh
Debashis Barik
Ananta Prasad Arukha
Sujata Prasad
Iteeshree Mohapatra
Amar Singh
Gatikrushna Singh
author_facet Shilpi Singh
Debashis Barik
Ananta Prasad Arukha
Sujata Prasad
Iteeshree Mohapatra
Amar Singh
Gatikrushna Singh
author_sort Shilpi Singh
collection DOAJ
description Conventional and cancer immunotherapies encompass diverse strategies to address various cancer types and stages. However, combining these approaches often encounters limitations such as non-specific targeting, resistance development, and high toxicity, leading to suboptimal outcomes in many cancers. The tumor microenvironment (TME) is orchestrated by intricate interactions between immune and non-immune cells dictating tumor progression. An innovative avenue in cancer therapy involves leveraging small molecules to influence a spectrum of resistant cell populations within the TME. Recent discoveries have unveiled a phenotypically diverse cohort of innate-like T (ILT) cells and tumor hybrid cells (HCs) exhibiting novel characteristics, including augmented proliferation, migration, resistance to exhaustion, evasion of immunosurveillance, reduced apoptosis, drug resistance, and heightened metastasis frequency. Leveraging small-molecule immunomodulators to target these immune players presents an exciting frontier in developing novel tumor immunotherapies. Moreover, combining small molecule modulators with immunotherapy can synergistically enhance the inhibitory impact on tumor progression by empowering the immune system to meticulously fine-tune responses within the TME, bolstering its capacity to recognize and eliminate cancer cells. This review outlines strategies involving small molecules that modify immune cells within the TME, potentially revolutionizing therapeutic interventions and enhancing the anti-tumor response.
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spelling doaj.art-9fc678266de24a828ca4f13cafd80f5f2023-11-19T15:44:41ZengMDPI AGBiomedicines2227-90592023-09-011110262110.3390/biomedicines11102621Small Molecule Targeting Immune Cells: A Novel Approach for Cancer TreatmentShilpi Singh0Debashis Barik1Ananta Prasad Arukha2Sujata Prasad3Iteeshree Mohapatra4Amar Singh5Gatikrushna Singh6Department of Neurosurgery, University of Minnesota, Minneapolis, MN 55455, USACenter for Computational Natural Science and Bioinformatics, International Institute of Information Technology, Hyderabad 500032, Telangana, IndiaDepartment of Neurosurgery, University of Minnesota, Minneapolis, MN 55455, USAMLM Medical Labs, LLC, Oakdale, MN 55128, USADepartment of Veterinary and Biomedical Sciences, University of Minnesota—Twin Cities, Saint Paul, MN 55108, USASchulze Diabetes Institute, Department of Surgery, University of Minnesota, Minneapolis, MN 55455, USADepartment of Neurosurgery, University of Minnesota, Minneapolis, MN 55455, USAConventional and cancer immunotherapies encompass diverse strategies to address various cancer types and stages. However, combining these approaches often encounters limitations such as non-specific targeting, resistance development, and high toxicity, leading to suboptimal outcomes in many cancers. The tumor microenvironment (TME) is orchestrated by intricate interactions between immune and non-immune cells dictating tumor progression. An innovative avenue in cancer therapy involves leveraging small molecules to influence a spectrum of resistant cell populations within the TME. Recent discoveries have unveiled a phenotypically diverse cohort of innate-like T (ILT) cells and tumor hybrid cells (HCs) exhibiting novel characteristics, including augmented proliferation, migration, resistance to exhaustion, evasion of immunosurveillance, reduced apoptosis, drug resistance, and heightened metastasis frequency. Leveraging small-molecule immunomodulators to target these immune players presents an exciting frontier in developing novel tumor immunotherapies. Moreover, combining small molecule modulators with immunotherapy can synergistically enhance the inhibitory impact on tumor progression by empowering the immune system to meticulously fine-tune responses within the TME, bolstering its capacity to recognize and eliminate cancer cells. This review outlines strategies involving small molecules that modify immune cells within the TME, potentially revolutionizing therapeutic interventions and enhancing the anti-tumor response.https://www.mdpi.com/2227-9059/11/10/2621immunotherapytumor microenvironmentinnate-like cellskiller innate-like T cellshybrid cellstissue-resident memory T cells
spellingShingle Shilpi Singh
Debashis Barik
Ananta Prasad Arukha
Sujata Prasad
Iteeshree Mohapatra
Amar Singh
Gatikrushna Singh
Small Molecule Targeting Immune Cells: A Novel Approach for Cancer Treatment
Biomedicines
immunotherapy
tumor microenvironment
innate-like cells
killer innate-like T cells
hybrid cells
tissue-resident memory T cells
title Small Molecule Targeting Immune Cells: A Novel Approach for Cancer Treatment
title_full Small Molecule Targeting Immune Cells: A Novel Approach for Cancer Treatment
title_fullStr Small Molecule Targeting Immune Cells: A Novel Approach for Cancer Treatment
title_full_unstemmed Small Molecule Targeting Immune Cells: A Novel Approach for Cancer Treatment
title_short Small Molecule Targeting Immune Cells: A Novel Approach for Cancer Treatment
title_sort small molecule targeting immune cells a novel approach for cancer treatment
topic immunotherapy
tumor microenvironment
innate-like cells
killer innate-like T cells
hybrid cells
tissue-resident memory T cells
url https://www.mdpi.com/2227-9059/11/10/2621
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