Investigating Therapies Targeting Druggable Targets of Mitochondria: Exploring the Efficacy for the Treatment of Cancer

Author:

Kumar Goel Kapil1,Rawat Pramod23,Murti Yogesh4,Mahajan Shriya5,Kandhari Harsimrat6,Kumar Bhupinder7,Ranjan Dwivedi Ashish8ORCID

Affiliation:

1. Department of Pharmaceutical Sciences Gurukul Kangri (Deemed to Be University) Haridwar, Uttarakhand 249404 India

2. Graphic Era (Deemed to be University) Clement Town Dehradun 248002 India

3. Graphic Era Hill University Clement Town Dehradun 248002 India

4. Institute of Pharmaceutical Research GLA University Mathura 281406 India

5. Centre of Research Impact and Outcome Chitkara University Rajpura, Punjab 140417 India

6. Chitkara Centre for Research and Development Chitkara University Himachal Pradesh 174103 India

7. Department of Medicinal Chemistry GITAM School of Pharmacy Hyderabad campus GITAM University Hyderabad 502329 India

8. GITAM School of Pharmacy GITAM (Deemed to be) University Hyderabad 502329 India Email

Abstract

AbstractCancer is a growing problem that has not yet been fully harnessed. Frequent mutations make this a highly variable and challenging pathology. Interestingly, mitochondria have currently emerged as a new target for cancer therapy. A group of agents with anticancer activity, termed mitocans that encourage apoptosis through mitochondrial disruption is currently important in research. From conventional glycolytic inhibitors to recent radiolabeled compounds, mitochondrial‐targeted therapies have marked their presence in cancer. Several TCA cycle and OXPHOS inhibitors are being established for their possible anticancer properties. There are so many distinctive differences in mitochondrial structure and function between normal and cancer cells that offer the potential for the clinical use of mitochondria as targets for novel and site‐specific anticancer agents. Mitochondrial targeting can be made possible if the bioactive molecule is specifically and selectively delivered to the mitochondria of the correct cell type using cell‐specific ligands and mitochondriotropic molecules.

Publisher

Wiley

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