Related Experiment Video
Updated: Apr 19, 2026

From a 2DE-Gel Spot to Protein Function: Lesson Learned From HS1 in Chronic Lymphocytic Leukemia
Published on: October 19, 2014
Targeting protein-protein interactions in hematologic malignancies: still a challenge or a great opportunity for
Tomasz Cierpicki1, Jolanta Grembecka
1Department of Pathology, University of Michigan, Ann Arbor, MI, USA.
Abstract:
Over the past several years, there has been an increasing research effort focused on inhibition of protein-protein interactions (PPIs) to develop novel therapeutic approaches for cancer, including hematologic malignancies. These efforts have led to development of small molecule inhibitors of PPIs, some of which already advanced to the stage of clinical trials while others are at different stages of preclinical optimization, emphasizing PPIs as an emerging and attractive class of drug targets. Here, we review several examples of recently developed inhibitors of PPIs highly relevant to hematologic cancers. We address the existing skepticism about feasibility of targeting PPIs and emphasize potential therapeutic benefit from blocking PPIs in hematologic malignancies. We then use these examples to discuss the approaches for successful identification of PPI inhibitors and provide analysis of the protein-protein interfaces, with the goal to address 'druggability' of new PPIs relevant to hematology. We discuss lessons learned to improve the success of targeting new PPIs and evaluate prospects and limits of the research in this field. We conclude that not all PPIs are equally tractable for blocking by small molecules, and detailed analysis of PPI interfaces is critical for selection of those with the highest chance of success. Together, our analysis uncovers patterns that should help to advance drug discovery in hematologic malignancies by successful targeting of new PPIs.
Insights
Targeting protein-protein interactions (PPIs) with small molecules offers a promising strategy for treating hematologic cancers. Careful analysis of PPI interfaces is crucial for successful drug discovery in this area.
Area of Science:
- Oncology
- Pharmacology
- Biochemistry
Background:
- Protein-protein interactions (PPIs) are increasingly recognized as viable drug targets for cancer therapy.
- Small molecule inhibitors of PPIs are advancing through preclinical and clinical development for hematologic malignancies.
Purpose of the Study:
- To review recent inhibitors of PPIs relevant to hematologic cancers.
- To discuss strategies for identifying and developing PPI inhibitors.
- To analyze the 'druggability' of PPIs in hematology.
Main Methods:
- Review of recently developed small molecule inhibitors of PPIs.
- Analysis of protein-protein interfaces to assess druggability.
- Evaluation of lessons learned and prospects in PPI inhibitor research.
Main Results:
- PPIs represent an emerging and attractive class of drug targets for hematologic cancers.
- Successful identification of PPI inhibitors requires careful analysis of protein-protein interfaces.
- Not all PPIs are equally amenable to small molecule inhibition.
Conclusions:
- Targeting PPIs holds significant therapeutic potential for hematologic malignancies.
- Detailed interface analysis is critical for selecting tractable PPI targets.
- This research provides insights to advance drug discovery for hematologic cancers by targeting PPIs.
More Related Videos
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
Targeted Cancer Therapies
Protein Networks
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
Protein-protein Interfaces
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...
Role of Hematopoietic Growth Factors
Thrombopoietin (TPO), mainly released by the liver,...

