Literature DB >> 20837837

Association between pharmaceutical support and basic science research on erythropoiesis-stimulating agents.

Charles L Bennett1, Stephen Y Lai, Michael Henke, Sara E Barnato, James O Armitage, Oliver Sartor.   

Abstract

BACKGROUND: To our knowledge, no prior research has evaluated the association between pharmaceutical industry funding and basic science research results. When erythropoiesis-stimulating agents (ESAs) were licensed to treat chemotherapy-associated anemia, basic science concerns related to potential cancer stimulation were raised. We evaluated associations between pharmaceutical industry support and reported findings evaluating ESA effects on cancer cells.
METHODS: Articles identified in MEDLINE and EMBASE databases (1988-2008) investigating basic science findings related to ESA administration in the solid tumor setting were reviewed. Outcomes included information on erythropoietin receptors (EpoRs), Epo-induced signaling events, cellular function, and qualitative conclusions. Information on study funding (academic investigators with no reported funding from ESA manufacturers [64 studies], academic investigators with grant funding from ESA manufacturers [7 studies], and investigators employed by the ESA manufacturers [3 studies]) was evaluated. Some studies did not include information on each outcome.
RESULTS: Investigators without funding from ESA manufacturers were more likely than academic investigators with such funding or investigators employed by ESA manufacturers to identify EpoRs on solid tumor cells (100%, 60%, and 67%, respectively; P = .009), Epo-induced signaling events (94%, 0%, and 0%, respectively; P = .001), or changes in cellular function (57%, 0%, and 0%, respectively; P = .007) and to conclude that ESAs had potentially harmful effects on cancer cells (57%, 0%, and 0%, respectively; P = .008).
CONCLUSIONS: Researchers who do not have pharmaceutical industry support are more likely than those with pharmaceutical support to identify detrimental in vitro effects of ESAs. The potential for conflicts of interest to affect basic science research should be considered.

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Year:  2010        PMID: 20837837      PMCID: PMC4138541          DOI: 10.1001/archinternmed.2010.309

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN: 0003-9926


  87 in total

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3.  The effect of human recombinant erythropoietin on the growth of a human neuroblastoma cell line.

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4.  Erythropoietin modulates intracellular calcium in a human neuroblastoma cell line.

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Journal:  Gynecol Oncol       Date:  1999-05       Impact factor: 5.482

6.  Hypoxia-induced erythropoietin expression in human neuroblastoma requires a methylation free HIF-1 binding site.

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7.  Erythropoietin-induced reduction of hypoxia before and during fractionated irradiation contributes to improvement of radioresponse in human glioma xenografts.

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Journal:  Zentralbl Pathol       Date:  1992-09

9.  Autocrine erythropoietin signaling inhibits hypoxia-induced apoptosis in human breast carcinoma cells.

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Authors:  Geza Acs; Xiaowei Xu; Christina Chu; Peter Acs; Ajay Verma
Journal:  Cancer       Date:  2004-06-01       Impact factor: 6.860

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6.  How basic scientists help the pharmaceutical industry market drugs.

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Review 7.  Effects of erythropoiesis-stimulating agents on fatigue- and anaemia-related symptoms in cancer patients: systematic review and meta-analyses of published and unpublished data.

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8.  Erythropoiesis-stimulating agents and quality of life: personal journeys of a cancer survivor, oncologist, and two cancer health services researchers.

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