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Could drugs inhibiting the mevalonate pathway also target cancer stem cells?

Likus, Wirginia (författare)
Medical University of Silesia, Poland
Siemianowicz, Krzysztof (författare)
Medical University of Silesia, Poland
Bienk, Konrad (författare)
Aarhus University, Denmark
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Pakula, Malgorzata (författare)
Aarhus University, Denmark
Pathak, Himani (författare)
Indian Institute Science Educ and Research IISER TVM, India
Dutta, Chhanda (författare)
Linköpings universitet,Medicinska fakulteten,Avdelningen för cellbiologi
Wang, Qiong (författare)
Linköpings universitet,Teknisk biologi,Tekniska fakulteten
Shojaei, Shahla (författare)
Isfahan University of Medical Science, Iran
Assaraf, Yehuda G. (författare)
Technion Israel Institute Technology, Israel
Ghavami, Saeid (författare)
University of Manitoba, Canada; Shiraz University of Medical Science, Iran
Cieslar-Pobuda, Artur (författare)
Silesian Technical University, Poland
Los, Marek J. (författare)
LinkoCare Life Science AB, S-58330 Linkoping, Sweden; Medical University of Silesia, Poland
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 (creator_code:org_t)
CHURCHILL LIVINGSTONE, 2016
2016
Engelska.
Ingår i: Drug resistance updates. - : CHURCHILL LIVINGSTONE. - 1368-7646 .- 1532-2084. ; 25, s. 13-25
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
Stäng  
  • Understanding the connection between metabolic pathways and cancer is very important for the development of new therapeutic approaches based on regulatory enzymes in pathways associated with tumorigenesis. The mevalonate cascade and its rate-liming enzyme HMG CoA-reductase has recently drawn the attention of cancer researchers because strong evidences arising mostly from epidemiologic studies, show that it could promote transformation. Hence, these studies pinpoint HMG CoA-reductase as a candidate proto-oncogene. Several recent epidemiological studies, in different populations, have proven that statins are beneficial for the treatment-outcome of various cancers, and may improve common cancer therapy strategies involving alkylating agents, and antimetabolites. Cancer stem cells/cancer initiating cells (CSC) are key to cancer progression and metastasis. Therefore, in the current review we address the different effects of statins on cancer stem cells. The mevalonate cascade is among the most pleiotropic, and highly interconnected signaling pathways. Through G-protein-coupled receptors (GRCP), it integrates extra-, and intracellular signals. The mevalonate pathway is implicated in cell sternness, cell proliferation, and organ size regulation through the Hippo pathway (e.g. Yap/Taz signaling axis). This pathway is a prime preventive target through the administration of statins for the prophylaxis of obesity related cardiovascular diseases. Its prominent role in regulation of cell growth and sternness also invokes its role in cancer development and progression. The mevalonate pathway affects cancer metastasis in several ways by: (i) affecting epithelial-to-mesenchymal transition (EMT), (ii) affecting remodeling of the cytoskeleton as well as cell motility, (iii) affecting cell polarity (non-canonical Wnt/planar pathway), and (iv) modulation of mesenchymal-to-epithelial transition (MET). Herein we provide an overview of the mevalonate signaling network. We then briefly highlight diverse functions of various elements of this mevalonate pathway. We further discuss in detail the role of elements of the mevalonate cascade in sternness, carcinogenesis, cancer progression, metastasis and maintenance of cancer stem cells. (C) 2016 The Authors. Published by Elsevier Ltd.

Ämnesord

NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)

Nyckelord

Cancer stem-like cells; Mevalonate cascade; Ras; Rho; Stemness; Statins; Yap

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