Related Experiment Video
Updated: Jul 9, 2026

Methods for Evaluating the Role of c-Fos and Dusp1 in Oncogene Dependence
Published on: January 7, 2019
Oncogene addiction: setting the stage for molecularly targeted cancer therapy
Sreenath V Sharma1, Jeffrey Settleman
1Center for Molecular Therapeutics, Massachusetts General Hospital Cancer Center and Harvard Medical School, Charlestown, Massachusetts 02129, USA.
Abstract:
In pugilistic parlance, the one-two punch is a devastating combination of blows, with the first punch setting the stage and the second delivering the knock-out. This analogy can be extended to molecularly targeted cancer therapies, with oncogene addiction serving to set the stage for tumor cell killing by a targeted therapeutic agent. While in vitro and in vivo examples abound documenting the existence of this phenomenon, the mechanistic underpinnings that govern oncogene addiction are just beginning to emerge. Our current inability to fully exploit this weakness of cancer cells stems from an incomplete understanding of oncogene addiction, which nonetheless represents one of the rare chinks in the formidable armor of cancer cells.
Insights
Cancer cells rely on oncogene addiction, a vulnerability that primes them for targeted therapies. Understanding this mechanism is key to developing effective treatments and exploiting this weakness.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Cancer cells often exhibit oncogene addiction, a dependence on specific oncogenes for survival and proliferation.
- This addiction creates a vulnerability that can be exploited by molecularly targeted therapies.
- Despite evidence, the underlying mechanisms of oncogene addiction are not fully understood.
Purpose of the Study:
- To explore the concept of oncogene addiction as a vulnerability in cancer therapy.
- To highlight the importance of understanding the mechanistic underpinnings of oncogene addiction.
- To emphasize the potential of targeting oncogene addiction for cancer treatment.
Main Methods:
- This study is a conceptual review, drawing parallels with established principles in molecular biology and cancer research.
- It synthesizes existing knowledge on oncogene addiction from in vitro and in vivo studies.
- The approach involves extending the analogy of a 'one-two punch' to explain therapeutic strategies.
Main Results:
- Oncogene addiction acts as the 'first punch,' sensitizing cancer cells to targeted agents.
- Targeted therapeutic agents deliver the 'knock-out' by exploiting this addiction.
- The phenomenon is well-documented but its mechanistic details require further elucidation.
Conclusions:
- Oncogene addiction represents a critical weakness in cancer cells.
- A deeper understanding of oncogene addiction mechanisms is essential for advancing cancer therapy.
- Exploiting oncogene addiction holds significant promise for developing effective molecularly targeted treatments.
More Related Videos
10:27Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
09:37Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells
Published on: August 25, 2021
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...
Cancer-Critical Genes I: Proto-oncogenes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
Cancer-Critical Genes I: Proto-oncogenes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
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...
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...