Publications by authors named "Deepan Chatterjee"

Unlabelled: Small cell lung carcinoma (SCLC) tumors are heterogeneous, with a subpopulation of cells primed for tumor initiation. In this study, we show that kinase suppressor of Ras 2 (KSR2) promotes the self-renewal and clonogenicity of SCLC cells. KSR2 is a molecular scaffold that promotes Raf/MEK/ERK signaling.

View Article and Find Full Text PDF

Unlabelled: Small cell lung cancer (SCLC) has a dismal 5-year survival rate of less than 7%, with limited advances in first-line treatment over the past four decades. Tumor-initiating cells (TIC) contribute to resistance and relapse, a major impediment to SCLC treatment. In this study, we identify kinase suppressor of Ras 1 (KSR1), a molecular scaffold for the Raf/MEK/ERK signaling cascade, as a critical regulator of SCLC TIC formation and tumor initiation in vivo.

View Article and Find Full Text PDF
Article Synopsis
  • Acquired resistance to targeted cancer therapies significantly contributes to patient mortality, prompting the need for better resistance modeling.
  • The study introduces a 6-to-16-week assay for simulating acquired resistance in both adherent and suspension cancer cell lines, focusing on testing dosages and combination therapies.
  • This protocol offers a high-throughput, scalable, and cost-effective approach for researching drug resistance, with full details available in referenced studies by Sealover et al. and Theard et al.
View Article and Find Full Text PDF

Unlabelled: Small-cell lung cancer (SCLC) has a dismal five-year survival rate of less than 7%, with limited advances in first line treatment over the past four decades. Tumor-initiating cells (TICs) contribute to resistance and relapse, a major impediment to SCLC treatment. Here, we identify Kinase Suppressor of Ras 1 (KSR1), a molecular scaffold for the Raf/MEK/ERK signaling cascade, as a critical regulator of SCLC TIC formation and tumor initiation .

View Article and Find Full Text PDF

KRAS is the most commonly mutated oncogene. Targeted therapies have been developed against mediators of key downstream signaling pathways, predominantly components of the RAF/MEK/ERK kinase cascade. Unfortunately, single-agent efficacy of these agents is limited both by intrinsic and acquired resistance.

View Article and Find Full Text PDF