Literature DB >> 11000097

Sodium arsenite inhibits terminal differentiation of murine C3H 10T1/2 preadipocytes.

K J Trouba1, E M Wauson, R L Vorce.   

Abstract

Cancer represents an imbalance between cell proliferation and differentiation, two processes that are coordinately and antagonistically regulated. Aberrant cell proliferation is considered to be an important etiological factor in the development of arsenic-induced cancer, suggesting that arsenic also dysregulates differentiation. Based on evidence that arsenic modulates mitogenic events that antagonize the process of differentiation, this study addresses the hypothesis that sodium arsenite inhibits insulin/dexamethasone-induced differentiation of C3H 10T1/2 preadipocytes; it was further postulated that arsenic-treated cells retain mitogenic responsiveness under differentiating conditions. To test this hypothesis, the differentiation capacity of C3H 10T1/2 preadipocytes was examined in control cells and cells treated with sodium arsenite. Differentiation was assessed morphologically and quantified by Oil Red-O staining of accumulated lipids. The effect of long-term arsenic exposure on mitogenic competence was quantified by flow cytometry, [(3)H]thymidine incorporation, and cell counting under conditions favorable for adipocyte differentiation. Results indicate that arsenic inhibits morphological differentiation of wild-type C3H 10T1/2 preadipocytes. Short-term arsenic exposure inhibits differentiation in a dose-dependent manner, with arsenic concentrations > or = 3 microM producing a significant inhibition of dexamethasone/insulin-induced lipid accumulation. Furthermore, arsenic-treated cells exhibit an accentuated response to mitogenic stimulation under differentiating conditions. These data suggest that arsenic exposure results in the inhibition of cellular programming required for terminal differentiation of C3H 10T1/2 preadipocytes and that cells acquire mitogenic hyperresponsiveness. The ability of arsenic to dysregulate the balance between proliferation and differentiation is proposed to be one mechanism by which this metalloid causes cancer in humans. Copyright 2000 Academic Press.

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Year:  2000        PMID: 11000097     DOI: 10.1006/taap.2000.9012

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  14 in total

1.  Chronic exposure to low-dose arsenic modulates lipogenic gene expression in mice.

Authors:  Adeola O Adebayo; Fokko Zandbergen; Courtney D Kozul-Horvath; Philip A Gruppuso; Joshua W Hamilton
Journal:  J Biochem Mol Toxicol       Date:  2014-08-23       Impact factor: 3.642

2.  Oxidation state specific analysis of arsenic species in tissues of wild-type and arsenic (+3 oxidation state) methyltransferase-knockout mice.

Authors:  Jenna M Currier; Christelle Douillet; Zuzana Drobná; Miroslav Stýblo
Journal:  J Environ Sci (China)       Date:  2016-07-18       Impact factor: 5.565

3.  An isolated cryptic peptide influences osteogenesis and bone remodeling in an adult mammalian model of digit amputation.

Authors:  Vineet Agrawal; Jeremy Kelly; Stephen Tottey; Kerry A Daly; Scott A Johnson; Bernard F Siu; Janet Reing; Stephen F Badylak
Journal:  Tissue Eng Part A       Date:  2011-08-29       Impact factor: 3.845

4.  Arsenic exposure perturbs epithelial-mesenchymal cell transition and gene expression in a collagen gel assay.

Authors:  Alejandro Lencinas; Derrick M Broka; Jay H Konieczka; Scott E Klewer; Parker B Antin; Todd D Camenisch; Raymond B Runyan
Journal:  Toxicol Sci       Date:  2010-03-22       Impact factor: 4.849

5.  Associations between rice consumption, arsenic metabolism, and insulin resistance in adults without diabetes.

Authors:  Xiang Li; Xin Wang; Sung Kyun Park
Journal:  Int J Hyg Environ Health       Date:  2021-09-03       Impact factor: 7.401

6.  Arsenic inhibits myogenic differentiation and muscle regeneration.

Authors:  Yuan-Peng Yen; Keh-Sung Tsai; Ya-Wen Chen; Chun-Fa Huang; Rong-Sen Yang; Shing-Hwa Liu
Journal:  Environ Health Perspect       Date:  2010-03-18       Impact factor: 9.031

7.  Characterization of the impaired glucose homeostasis produced in C57BL/6 mice by chronic exposure to arsenic and high-fat diet.

Authors:  David S Paul; Felecia S Walton; R Jesse Saunders; Miroslav Stýblo
Journal:  Environ Health Perspect       Date:  2011-05-18       Impact factor: 9.031

8.  Association between arsenic suppression of adipogenesis and induction of CHOP10 via the endoplasmic reticulum stress response.

Authors:  Yongyong Hou; Peng Xue; Courtney G Woods; Xia Wang; Jingqi Fu; Kathy Yarborough; Weidong Qu; Qiang Zhang; Melvin E Andersen; Jingbo Pi
Journal:  Environ Health Perspect       Date:  2012-12-05       Impact factor: 9.031

Review 9.  Evaluation of the association between arsenic and diabetes: a National Toxicology Program workshop review.

Authors:  Elizabeth A Maull; Habibul Ahsan; Joshua Edwards; Matthew P Longnecker; Ana Navas-Acien; Jingbo Pi; Ellen K Silbergeld; Miroslav Styblo; Chin-Hsiao Tseng; Kristina A Thayer; Dana Loomis
Journal:  Environ Health Perspect       Date:  2012-08-10       Impact factor: 9.031

10.  Cellular stress alters 3'UTR landscape through alternative polyadenylation and isoform-specific degradation.

Authors:  Dinghai Zheng; Ruijia Wang; Qingbao Ding; Tianying Wang; Bingning Xie; Lu Wei; Zhaohua Zhong; Bin Tian
Journal:  Nat Commun       Date:  2018-06-11       Impact factor: 14.919

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