International Journal of Clinical Medicine

Volume 2, Issue 4 (September 2011)

ISSN Print: 2158-284X   ISSN Online: 2158-2882

Google-based Impact Factor: 0.52  Citations  h5-index & Ranking

Mitocans as Novel Agents for Anticancer Therapy: An Overview

HTML  Download Download as PDF (Size: 602KB)  PP. 515-529  
DOI: 10.4236/ijcm.2011.24086    7,483 Downloads   13,721 Views  Citations

Affiliation(s)

.

ABSTRACT

Many conventional anticancer drugs have an associated lack of safety by their toxicity. Relatively faster mutations in tumor cells pose a significant obstacle in treatment of cancer. Recently, “Mitocans” have emerged as a novel class of anticancer agents selectively targeting tumor cells and thus, are much less toxic than conventional anticancer chemotherapeutic agents. Mitocans are drugs that act directly on mitochondria within the cell, thus causing changes in energy metabolism of the cell. Amongst these mitocans, α-Tocopheryl succinate or vitamin E analogs are studied very well by researchers. This review discusses mitochondrial drug targeting strategies and a variety of novel mitochondrial drug targets of mitocans, such as electron transport chain, mitochondrial permeability transition, Bcl-2 family proteins and mitochondrial DNA. The purpose of this review is to focus on the various classes of mitocans, the mechanisms by which these drugs specifically act on tumor cells and their applications in cancer chemotherapeutics.

Share and Cite:

V. Panda, P. Khambat and S. Patil, "Mitocans as Novel Agents for Anticancer Therapy: An Overview," International Journal of Clinical Medicine, Vol. 2 No. 4, 2011, pp. 515-529. doi: 10.4236/ijcm.2011.24086.

Cited by

[1] A peptide-derived strategy for specifically targeting the mitochondria and ER of cancer cells: a new approach in fighting cancer
Chemical …, 2022
[2] Gold (I) Complexes Bearing Alkylated 1, 3, 5-Triaza-7-phosphaadamantane Ligands as Thermoresponsive Anticancer Agents in Human Colon Cells
Biomedicines, 2021
[3] Design, synthesis and biological evaluation of dihydro-2-quinolone platinum (IV) hybrids as antitumor agents displaying mitochondria injury and DNA damage …
2021
[4] Type and position of linkage govern the cytotoxicity of oleanolic acid rhodamine B hybrids
2021
[5] Cytotoxic triterpenoid–safirinium conjugates target the endoplasmic reticulum
2020
[6] Novel Pt (IV) Prodrugs Displaying Antimitochondrial Effects
2020
[7] TPP-based mitocans: a potent strategy for anticancer drug design
2020
[8] Targeting Mitochondria Through the Use of Mitocans as Emerging Anticancer Agents
2019
[9] Αντικαρκινικά οργανομεταλλικά σύμπλοκα του Ru (II)
2018
[10] Mitochondria-Targeting Anticancer Metal Complexes
2018
[11] Mitochondria-localizing BODIPY–copper (ii) conjugates for cellular imaging and photo-activated cytotoxicity forming singlet oxygen
Dalton Transactions, 2018
[12] Targeting mitochondria: Esters of rhodamine B with triterpenoids are mitocanic triggers of apoptosis
European Journal of Medicinal Chemistry, 2018
[13] An X-ray and Natural Bond Orbital (NBO) structural study of α-tocopheryl and 2, 2, 5, 7, 8-pentamethylchroman-6-yl succinates
Journal of Saudi Chemical Society, 2018
[14] Rhodamine B conjugates of triterpenoic acids are cytotoxic mitocans even at nanomolar concentrations
European Journal of Medicinal Chemistry, 2017
[15] TRITERPEN-CARBONSÄURE-DERIVATEN
Dissertation, 2017
[16] Synthese und biologische Evaluierung von Triterpen-Carbonsäure-Derivaten
2017
[17] Guanidine-Based DNA Binders and Strategies Toward their Platinum Complexes as Anticancer Dual Agents
2016
[18] Mitochondrial permeability transition as target of anticancer drugs
Current pharmaceutical design, 2014
[19] First Spin-Labeled α-Tocopherol and Trolox Succinyl Derivatives
Chemistry of Natural Compounds, 2014
[20] Conjugates of Natural Compounds with Nitroxyl Radicals as a Basis for Creation of Pharmacological Agents of New Generation
Current medicinal chemistry, 2014
[21] Studies Of The Antifungal And Anticancer Properties Of Hevea Brasiliensis Latex B-Serum And Their Sub-Fractions
2013

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.