CHEMOTHERAPY AND CANCER CELLS - SCI & TECH

News: How do some cancer cells survive chemotherapy? Scientists find one way

 

What's in the news?

       Researchers at the Netherlands Cancer Institute have conducted a recent study to investigate drug resistance in cancer cells, focusing on resistance to a drug known as Taxol.

       It studied Chemotherapy and cancer relapse, particularly when a small number of cancer cells resist treatment and remain dormant, potentially leading to a resurgence of the disease.

 

Chemotherapy and its limitations:

       Cancer cells are characterized by uncontrolled and rapid division.

       Chemotherapeutic drugs aim to halt this proliferation, often triggering programmed cell death, known as apoptosis, in response to halted cell division.

       However, this approach also damages healthy dividing cells, leading to adverse side effects.

 

Fine-Tuning Cancer Treatment:

       Oncologists face the challenge of finding an effective drug dose that eliminates cancer cells while minimizing unbearable side effects for patients.

       One approach has been the development of antibody-drug conjugates (ADCs) that target specific proteins found mainly on cancer cells, sparing non-cancerous cells.

 

Unraveling Drug Resistance:

1. P-gp Protein: 

       Some cancer cells escape drug treatments by overexpressing a protein called P-gp (permeability glycoprotein), which acts as a pump, expelling toxic compounds, including chemotherapeutic agents.

2. ABCB1 Gene: 

       The production of P-gp is controlled by the ABCB1 gene and cells that produce excessive P-gp can flush out chemotherapy drugs, preventing them from accumulating at levels needed to trigger apoptosis.

 

Role of Cellular Location:

1. Recent Findings: 

       The study examined the sensitivity of cells to Taxol and identified that the location of the ABCB1 gene within the cell’s nucleus plays a crucial role.

2. Nuclear Envelope: 

       In sensitive cells, the ABCB1 gene is located close to the nuclear envelope. In resistant cells, the gene has detached from the envelope and moved further inside the nucleus, resulting in a 100-fold increase in ABCB1 gene-related RNA.

3. Key Protein - Lamin B Receptor (LBR):

       LBR’s Influence - Researchers discovered that the presence or absence of a protein called Lamin B Receptor (LBR) affects the location of the ABCB1 gene.

 

       Depletion of LBR - When LBR is depleted, cells can activate the ABCB1 gene when exposed to Taxol. However, the absence of the LBR gene itself does not immediately increase ABCB1 expression, indicating the involvement of additional factors.

       Diverse Responses - Different cancer types exhibit varying responses to LBR depletion, highlighting the complex mechanisms governing gene expression and silencing.

 

Significance:

       These findings emphasize the need for further research into the diverse ways cancer cells express or suppress genes.

       Understanding drug resistance mechanisms opens avenues for developing strategies to maintain the potency of anti-cancer drugs while minimizing side effects, ultimately benefiting patients on their path to recovery.