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Sökning: (L773:0008 5472) srt2:(2010-2019) > (2019) > Heparanase Accelera...

Heparanase Accelerates Obesity-Associated Breast Cancer Progression

Hermano, Esther (författare)
Hadassah Hebrew Univ, Med Ctr, Sharett Inst Oncol, Jerusalem, Israel
Goldberg, Rachel (författare)
Hadassah Hebrew Univ, Med Ctr, Sharett Inst Oncol, Jerusalem, Israel
Rubinstein, Ariel M. (författare)
Hadassah Hebrew Univ, Med Ctr, Sharett Inst Oncol, Jerusalem, Israel
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Sonnenblick, Amir (författare)
Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Oncol Div, Tel Aviv, Israel; Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
Maly, Bella (författare)
Hadassah Hebrew Univ, Med Ctr, Dept Pathol, Jerusalem, Israel
Nahmias, Daniela (författare)
Hadassah Hebrew Univ, Med Ctr, Sharett Inst Oncol, Jerusalem, Israel
Li, Jin-Ping (författare)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Bakker, Marinka A. H. (författare)
Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, Dept Nephrol, Nephrol Res Lab,Med Ctr, Nijmegen, Netherlands
van der Vlag, Johan (författare)
Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, Dept Nephrol, Nephrol Res Lab,Med Ctr, Nijmegen, Netherlands
Vlodavsky, Israel (författare)
Technion, Rappaport Fac Med, Canc & Vasc Biol Res Ctr, Haifa, Israel
Peretz, Tamar (författare)
Hadassah Hebrew Univ, Med Ctr, Sharett Inst Oncol, Jerusalem, Israel; Hebrew Univ Jerusalem, Med Sch, Jerusalem, Israel
Elkin, Michael (författare)
Hadassah Hebrew Univ, Med Ctr, Sharett Inst Oncol, Jerusalem, Israel; Hebrew Univ Jerusalem, Med Sch, Jerusalem, Israel
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 (creator_code:org_t)
2019
2019
Engelska.
Ingår i: Cancer Research. - 0008-5472 .- 1538-7445. ; 79:20, s. 5342-5354
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Obese women have higher risk of bearing breast tumors that are highly aggressive and resistant to therapies. Tumor-promoting effects of obesity occur locally via adipose inflammation and related alterations to the extracellular matrix (ECM) as well as systemically via circulating metabolic mediators (e.g., free fatty acids, FFA) associated with excess adiposity and implicated in toll-like receptor-mediated activation of macrophages-key cellular players in obesity-related cancer progression. Although the contribution of macrophages to proneoplastic effects of obesity is well documented, the role of ECM components and their enzymatic degradation is less appreciated. We show that heparanase, the sole mammalian endoglucuronidase that cleaves heparan sulfate in ECM, is preferentially expressed in clinical/experimental obesity-associated breast tumors. Heparanase deficiency abolished obesity-accelerated tumor progression in vivo. Heparanase orchestrated a complex molecular program that occurred concurrently in adipose and tumor tissue and sustained the cancer-promoting action of obesity. Heparanase was required for adipose tissue macrophages to produce inflammatory mediators responsible for local induction of aromatase, a rate-limiting enzyme in estrogen biosynthesis. Estrogen upregulated heparanase in hormone-responsive breast tumors. In subsequent stages, elevated levels of heparanase induced acquisition of procancerous phenotype by tumor-associated macrophages, resulting in activation of tumor-promoting signaling and acceleration of breast tumor growth under obese conditions. As techniques to screen for heparanase expression in tumors become available, these findings provide rational and a mechanistic basis for designing antiheparanase approaches to uncouple obesity and breast cancer in a rapidly growing population of obese patients. Significance: This study reveals the role of heparanase in promoting obesity-associated breast cancer and provides a mechanistically informed approach to uncouple obesity and breast cancer in a rapidly growing population of obese patients.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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