Related Experiment Video
Updated: Jan 13, 2026

Preparation of Primary Acute Lymphoblastic Leukemia Cells in Different Cell Cycle Phases by Centrifugal Elutriation
Published on: November 10, 2017
Targeting cell cycle in leukemia: "Is palbociclib the game-changer?": A review
Muhamad Amir Azizan1, Zainul Abeden1, Nur Haida Natasha Shamsuddin1
1Department of Biomedical Science, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Kepala Batas, Pulau Pinang, Malaysia.
Abstract:
Leukemia is a complex and heterogeneous disease, making it challenging to determine the correct treatment. Over the past few decades, there have been few changes in standard medical care. To mitigate this problem, several potential small molecules that target the disease at the molecular level are being investigated for their clinical significance in leukemia treatment. Among them, the cyclin-dependent kinase (CDK) inhibitor palbociclib emerges as a promising therapeutic candidate targeting CDK4/6. Although palbociclib was approved by the Food and Drug Administration for the treatment of HER2-negative and HR-positive advanced or metastatic breast cancer, its potential in leukemia is still under research. Furthermore, CDK6 has been discovered to have essential roles in leukemic cells beyond its involvement in cell cycle progression, making it a notable target in leukemia. This review comprehensively analyses existing literature on the effectiveness and safety of using palbociclib alone or in combination with other treatments in preclinical and clinical leukemia investigations.
Insights
Palbociclib, a CDK4/6 inhibitor, shows promise for leukemia treatment. This review analyzes its effectiveness and safety in preclinical and clinical studies for this complex cancer.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Leukemia is a complex and heterogeneous cancer with limited treatment advancements.
- Targeting molecular pathways offers a promising strategy for novel leukemia therapies.
- Cyclin-dependent kinases (CDKs) are critical regulators of the cell cycle and are implicated in cancer progression.
Purpose of the Study:
- To review the existing literature on palbociclib's efficacy and safety in leukemia.
- To evaluate palbociclib as a therapeutic candidate targeting CDK4/6 in leukemia.
- To explore the role of CDK6 in leukemic cells beyond cell cycle progression.
Main Methods:
- Comprehensive literature analysis of preclinical and clinical studies.
- Investigation of palbociclib's mechanism of action as a CDK4/6 inhibitor.
- Assessment of palbociclib's efficacy as a monotherapy and in combination treatments.
Main Results:
- Palbociclib targets CDK4/6, showing potential in leukemia treatment.
- CDK6 plays crucial roles in leukemic cells, making it a significant therapeutic target.
- Existing literature suggests palbociclib's effectiveness and safety profile warrants further investigation in leukemia.
Conclusions:
- Palbociclib is a promising therapeutic agent for leukemia, particularly targeting CDK4/6.
- Further clinical investigations are needed to establish palbociclib's role in leukemia treatment regimens.
- Targeting CDK6 presents a viable strategy for developing novel leukemia therapies.
More Related Videos
Related Concept Videos
Inhibition of Cdk Activity
Targeted Cancer Therapies
There are several types of targeted therapies against...
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...
The Cell Cycle Control System
The Cell Cycle Control System
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
M-Cdk Drives Transition Into Mitosis
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...

