Adiponectin enhances Imatinib anti‐tumour activity in human chronic myeloid leukaemia cells with serum levels associated with Imatinib efficacy in early chronic phase patients. (August 2015)
- Record Type:
- Journal Article
- Title:
- Adiponectin enhances Imatinib anti‐tumour activity in human chronic myeloid leukaemia cells with serum levels associated with Imatinib efficacy in early chronic phase patients. (August 2015)
- Main Title:
- Adiponectin enhances Imatinib anti‐tumour activity in human chronic myeloid leukaemia cells with serum levels associated with Imatinib efficacy in early chronic phase patients
- Authors:
- Tan, Guangshan
Shi, Lei
Li, Qiang
Wang, Mingjun - Abstract:
- <abstract abstract-type="main" id="cpr12194-abs-0001"> <title>Abstract</title> <sec id="cpr12194-sec-0001" sec-type="section"> <title>Objectives</title> <p>Adiponectin, a functional ligand of adiponectin receptor‐1 (AdipoR1) and adiponectin receptor‐2 (AdipoR2), has been found to be linked to risk of development of chronic myeloid leukaemia (CML). Imatinib, as its first‐line therapy, exhibits striking activity in both chronic and accelerated phases of the condition. However, numerous clinical trials have shown that many patients become refractory or experience relapses. Thus, development of new, hopefully effective Imatinib‐based treatment strategies, are still needed.</p> </sec> <sec id="cpr12194-sec-0002" sec-type="section"> <title>Materials and methods</title> <p>Effects of recombinant adiponectin protein, in enhancing Imatinib anti‐tumour activities, in K562 and MEG‐01 CML cells, were examined <italic>in vitro</italic> and <italic>in vivo</italic>. Forty‐eight consecutive newly diagnosed adult patients with Bcr‐Abl‐positive CML, in the early chronic phase (ECP), were enrolled in the study. Imatinib efficacy, plasma adiponectin levels and their correlations were analysed.</p> </sec> <sec id="cpr12194-sec-0003" sec-type="section"> <title>Results</title> <p>Data presented here indicate that adiponectin enhanced Imatinib efficacy <italic>in vitro</italic> and <italic>in vivo</italic>. Furthermore, this augmented effect was due to inhibition of Bcr‐Abl tyrosine kinase<abstract abstract-type="main" id="cpr12194-abs-0001"> <title>Abstract</title> <sec id="cpr12194-sec-0001" sec-type="section"> <title>Objectives</title> <p>Adiponectin, a functional ligand of adiponectin receptor‐1 (AdipoR1) and adiponectin receptor‐2 (AdipoR2), has been found to be linked to risk of development of chronic myeloid leukaemia (CML). Imatinib, as its first‐line therapy, exhibits striking activity in both chronic and accelerated phases of the condition. However, numerous clinical trials have shown that many patients become refractory or experience relapses. Thus, development of new, hopefully effective Imatinib‐based treatment strategies, are still needed.</p> </sec> <sec id="cpr12194-sec-0002" sec-type="section"> <title>Materials and methods</title> <p>Effects of recombinant adiponectin protein, in enhancing Imatinib anti‐tumour activities, in K562 and MEG‐01 CML cells, were examined <italic>in vitro</italic> and <italic>in vivo</italic>. Forty‐eight consecutive newly diagnosed adult patients with Bcr‐Abl‐positive CML, in the early chronic phase (ECP), were enrolled in the study. Imatinib efficacy, plasma adiponectin levels and their correlations were analysed.</p> </sec> <sec id="cpr12194-sec-0003" sec-type="section"> <title>Results</title> <p>Data presented here indicate that adiponectin enhanced Imatinib efficacy <italic>in vitro</italic> and <italic>in vivo</italic>. Furthermore, this augmented effect was due to inhibition of Bcr‐Abl tyrosine kinase activity in an AdipoR1‐dependent way, while AdipoR2 was not involved. Most importantly, additional clinical data revealed that adiponectin plasma levels in CML ECP patients, correlated with Imatinib efficacy.</p> </sec> <sec id="cpr12194-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Adiponectin enhanced Imatinib anti‐tumour activity in human chronic myeloid leukaemia cells and its serum levels were associated with Imatinib efficacy, in early chronic phase patients.</p> </sec> </abstract> … (more)
- Is Part Of:
- Cell proliferation. Volume 48:Number 4(2015:Aug.)
- Journal:
- Cell proliferation
- Issue:
- Volume 48:Number 4(2015:Aug.)
- Issue Display:
- Volume 48, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 48
- Issue:
- 4
- Issue Sort Value:
- 2015-0048-0004-0000
- Page Start:
- 486
- Page End:
- 496
- Publication Date:
- 2015-08
- Subjects:
- Cell proliferation -- Periodicals
571.84 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2184 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cpr.12194 ↗
- Languages:
- English
- ISSNs:
- 0960-7722
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.854000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4200.xml