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Full-Text Articles in Medicine and Health Sciences

Oncolog, Volume 45, Number 06, June 2000, Kerry L. Wright, Margaret E. Goode, Jack Roth Md, Gary S. Clayman Md, Dds Jun 2000

Oncolog, Volume 45, Number 06, June 2000, Kerry L. Wright, Margaret E. Goode, Jack Roth Md, Gary S. Clayman Md, Dds

OncoLog MD Anderson's Report to Physicians (All issues)

  • Newly Organized Ophthalmology Section Expands Treatment of Ocular Malignancies
  • Turning Knowledge Into Effective Gene Therapies, by Jack A. Roth, MD, Professor, Department of Thoracic and Cardiovascular Surgery, and Gary S. Clayman, MD, DDS, Associate Professor, Head and Neck Surgery
  • Microarrays Reduce Time, Labor, and Cost of DNA Analysis
  • New DNA Microarray Technology Could Speed Up Discovery of the Genetic Causes of Lung Cancer
  • House Call: Virtual Health: Finding Reliable Medical Resources on the Internet
  • Clinical Practice Guidelines: Case Report: Ovarian Cancer
  • Protocols: Studies Aim to Detect and Treat Ocular Malignancies


Effect Of Receptor-Selective Retinoids On Growth And Differentiation Pathways In Mouse Melanoma Cells, Sejal H. Desai, Goran Boskovic, Linda L. Eastham, Marcia Dawson, Richard M. Niles May 2000

Effect Of Receptor-Selective Retinoids On Growth And Differentiation Pathways In Mouse Melanoma Cells, Sejal H. Desai, Goran Boskovic, Linda L. Eastham, Marcia Dawson, Richard M. Niles

Biochemistry and Microbiology

Treatment of B16 mouse melanoma cells with all-trans-retinoic acid (ATRA) results in inhibition of cell proliferation and induction of differentiation. Accompanying these events is an induction of retinoic acid receptor β (RARβ) expression, an increase in protein kinase Cα (PKCα) expression, and enhanced activator protein-1 (AP-1) transcriptional activity. These cells express nuclear RARα and RARγ and nuclear retinoid X receptors (RXR) α and β constitutively. We tested the ability of receptor-selective retinoids to induce the biochemical changes found in ATRA-treated melanoma cells and also tested their effectiveness in decreasing anchorage-dependent and -independent growth. The RXR-selective ligand (2E,4E)-6-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)-3,7-dimethyl-2,4,6-octatrienoic acid (SR11246) was …


Oncolog, Volume 45, Number 05, May 2000, Kerry L. Wright, Stephanie Deming, Gordon B. Mills Md, Phd May 2000

Oncolog, Volume 45, Number 05, May 2000, Kerry L. Wright, Stephanie Deming, Gordon B. Mills Md, Phd

OncoLog MD Anderson's Report to Physicians (All issues)

  • Early Detection of Melanoma Spread May Increase Survival Benefits of Adjuvant Therapy
  • No Easy Answers: Women at Increased Risk for Breast Cancer Face Difficult Choices
  • DiaLog: Understanding Risk: A Prerequisite for Making Informed Decisions, by Gordon B. Mills, MD, PhD, Chairman, Department of Molecular Therapeutics
  • House Call: Looking for Trouble: How to Spot Signs of Melanoma
  • Protocols: Melanoma Clinical Trials
  • Biochemotherapy Means Hope for Patients with Advanced Melanoma