Related Experiment Video
Updated: May 30, 2026

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
Targeting Mcl-1 for the therapy of cancer
Bridget A Quinn1, Rupesh Dash, Belal Azab
1Virginia Commonwealth University, School of Medicine, Department of Human and Molecular Genetics, Richmond, VA, USA. pbfisher@vcu.edu
Introduction:
Human cancers are genetically and epigenetically heterogeneous and have the capacity to commandeer a variety of cellular processes to aid in their survival, growth and resistance to therapy. One strategy is to overexpress proteins that suppress apoptosis, such as the Bcl-2 family protein Mcl-1. The Mcl-1 protein plays a pivotal role in protecting cells from apoptosis and is overexpressed in a variety of human cancers.
Areas Covered:
Targeting Mcl-1 for extinction in these cancers, using genetic and pharmacological approaches, represents a potentially effectual means of developing new efficacious cancer therapeutics. Here we review the multiple strategies that have been employed in targeting this fundamental protein, as well as the significant potential these targeting agents provide in not only suppressing cancer growth, but also in reversing resistance to conventional cancer treatments.
Expert Opinion:
We discuss the potential issues that arise in targeting Mcl-1 and other Bcl-2 anti-apoptotic proteins, as well problems with acquired resistance. The application of combinatorial approaches that involve inhibiting Mcl-1 and manipulation of additional signaling pathways to enhance therapeutic outcomes is also highlighted. The ability to specifically inhibit key genetic/epigenetic elements and biochemical pathways that maintain the tumor state represent a viable approach for developing rationally based, effective cancer therapies.
Insights
Targeting Mcl-1, a protein that helps cancer cells survive, offers a promising strategy for new cancer therapies. Inhibiting Mcl-1 can suppress tumor growth and overcome resistance to existing treatments.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Human cancers exhibit genetic and epigenetic heterogeneity, utilizing cellular processes for survival and therapeutic resistance.
- Overexpression of apoptosis-suppressing proteins, like Mcl-1 (Bcl-2 family), is a common cancer survival strategy.
- Mcl-1 plays a critical role in preventing apoptosis and is frequently overexpressed in various human cancers.
Purpose of the Study:
- To review strategies for targeting Mcl-1 (Myeloid cell leukemia 1) in cancer therapy.
- To highlight the potential of Mcl-1 targeting agents in suppressing tumor growth and reversing treatment resistance.
Main Methods:
- Review of genetic and pharmacological approaches targeting Mcl-1.
- Discussion of Mcl-1's role in apoptosis suppression and cancer progression.
- Analysis of challenges and combinatorial strategies for Mcl-1 inhibition.
Main Results:
- Targeting Mcl-1 presents a potentially effective therapeutic avenue for various human cancers.
- Inhibiting Mcl-1 can suppress cancer growth and enhance sensitivity to conventional therapies.
- Combinatorial approaches involving Mcl-1 inhibition show promise for improved therapeutic outcomes.
Conclusions:
- Targeting Mcl-1 and other anti-apoptotic Bcl-2 proteins faces challenges, including acquired resistance.
- Combinatorial strategies, involving Mcl-1 inhibition and pathway manipulation, can enhance therapeutic efficacy.
- Targeting key genetic/epigenetic elements and biochemical pathways offers a rational approach to effective cancer therapy.
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Mitogens and the Cell Cycle
Tumor Immunotherapy

