Article

New Method Slows Lung Cancer Tumor Growth

Protein inhibition shows promising reducing lung cancer progression.

By inhibiting a specific protein, researchers discovered a new way to impair tumor growth in lung cancer during a recent study.

Prior research demonstrates the differentiation factor C/EBPa acts as an important tumor suppressor in acute myelogenous leukemia and lung cancer. Furthermore, the loss of C/EBPa plays a role in the development of cancers, such as hepatic, squamous cell, and prostate cancer.

Although this information is known, the ways in which C/EBPa suppresses the formation of tumors was unknown. Researchers have continued to investigate C/EBPa in lung cancer, confirming that non-small cell lung cancer (NSCLC) frequently expresses low levels of C/EBPa, which results in poorer survival rates when corresponding with a reciprocally high expression of BMI1.

In a pre-clinical study published in Science Translational Medicine, researchers deleted C/EBPa, which resulted in NSCLC. Through the analysis of the study, researchers discovered that C/EBPa suppressed lung tumor formation by inhibiting the expression of BMI1.

Next, researchers demonstrated that reducing the levels of BMI1 by genetic means, or by using a drug reducing expression of BMI1, led to the inhibition of tumor formation.

“The study has established an important link between C/EBPa and BMI1 for the first time,” said lead researcher Daniel Tenen. “Furthermore, these findings suggest that assessment of expression levels of these proteins could be used as a way to predict which patients might benefit from drugs which inhibit BMI1, some of which are currently being evaluated in clinical trials.”

Related Videos
Anthony Perissinotti, PharmD, BCOP, discusses unmet needs and trends in managing chronic lymphocytic leukemia (CLL), with an emphasis on the pivotal role pharmacists play in supporting medication adherence and treatment decisions.
Image Credit: © alenamozhjer - stock.adobe.com
pharmacogenetics testing, adverse drug events, personalized medicine, FDA collaboration, USP partnership, health equity, clinical decision support, laboratory challenges, study design, education, precision medicine, stakeholder perspectives, public comment, Texas Medical Center, DNA double helix
pharmacogenetics challenges, inter-organizational collaboration, dpyd genotype, NCCN guidelines, meta census platform, evidence submission, consensus statements, clinical implementation, pharmacotherapy improvement, collaborative research, pharmacist role, pharmacokinetics focus, clinical topics, genotype-guided therapy, critical thought
Image Credit: © Andrey Popov - stock.adobe.com
Image Credit: © peopleimages.com - stock.adobe.com
TRUST-I and TRUST-II Trials Show Promising Results for Taletrectinib in ROS1+ NSCLC
World Standards Week 2024: US Pharmacopeia’s Achievements and Future Focus in Pharmacy Standards