Publications by authors named "Pablo E Puente"

Article Synopsis
  • - KRAS mutations are prevalent in lung adenocarcinoma among Black Americans, leading to the exploration of Polyisoprenylated Cysteinyl amide Inhibitors (PCAIs) as potential therapies to disrupt hyperactive G-protein signaling caused by mutated RAS proteins.
  • - Among 17 PCAIs tested, NSL-YHJ-2-27 and NSL-YHJ-2-46 demonstrated significant potency in affecting KRAS-mutated lung cancer cells, with EC50 values of 2.7 μM and 3.3 μM, and notable changes in MAPK pathway enzyme phosphorylation.
  • - Treatment with these PCAIs led to decreased levels of key G-proteins linked to cell migration
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Lung cancer is the leading cause of cancer death in the United States and worldwide, and a major source of cancer health disparities. Lung cancer cell lines provide key models for molecular studies of lung cancer development and progression, and for pre-clinical drug testing. To ensure health equity, it is imperative that cell lines representing different lung cancer histological types, carrying different cancer driver genes, and representing different genders, races, and ethnicities should be available.

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Synopsis of recent research by authors named "Pablo E Puente"

  • - Pablo E Puente's recent research focuses on understanding the implications of KRAS mutations in lung cancer, specifically targeting therapy that disrupts hyperactive G-protein signaling associated with these mutations.
  • - His study on polyisoprenylated cysteinyl amide inhibitors (PCAIs) demonstrates their potential to induce apoptosis and inhibit cell migration in KRAS-mutated lung adenocarcinoma cells derived from Black Americans.
  • - Puente highlights the critical lack of racial and ethnic diversity in lung cancer cell lines, stressing the need for more representative models to address health disparities and ensure equitable cancer treatment and drug testing.