کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5509456 | 1538515 | 2017 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Defining the Na+/H+ exchanger NHE1 interactome in triple-negative breast cancer cells
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کلمات کلیدی
PI3Kp160ROCKp90RSKNHE1PIP2ezrin-radixin-moesinACC1p38MAPKNF2GSKPDGFFOXO3aERMHER2ERK1/2 - ERK1 / 2p90 ribosomal S6 kinase - S6 kinase ribosomal p90Akt - آکتCAII - اسبacetyl-CoA carboxylase - استیل کروکسی سیلازforkhead box O3a - جعبه جعبه O3aplatelet-derived growth factor - فاکتور رشد حاصل از پلاکتphosphatidylinositol 4,5-biphosphate - فسفاتیدیلینوزیتول 4،5-بی فسفاتphosphoinositide-3-kinase - فسفونیوییدید-3-کینازneurofibromin 2 - نوروفیبرومین 2hemagglutinin - هماگلوتینینp38 mitogen-activated protein kinases - پروتئین کیناز متیوژن فعال P38carbonic anhydrase II - کربنیک آنیدراز IIextracellular signal-regulated kinase 1/2 - کیناز 1/2 تنظیم سیگنال خارج سلولیglycogen synthase kinase - گلیکوزین سیتستاز کینازEstrogen receptor - گیرنده استروژنHuman epidermal growth factor receptor 2 - گیرنده عامل فاکتور رشد اپیدرمی انسان 2Progesterone receptor - گیرنده پروژسترون
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Mounting evidence supports a major role for the Na+/H+ exchanger NHE1 in cancer progression and metastasis. NHE1 is hyperactive at the onset of oncogenic transformation, resulting in intracellular alkalinization and extracellular microenvironmental acidification. These conditions promote invasion and facilitate metastasis. However, the signal pathways governing the regulation of exchanger activity are still unclear. This is especially important in the aggressively metastatic, triple-negative basal breast cancer subtype. We used affinity chromatography followed by mass spectrometry to identify novel and putative interaction partners of NHE1 in MDA-MB-231 triple-negative breast cancer cells. NHE1 associated with several types of proteins including cytoskeletal proteins and chaperones. We validated protein interactions by co-immunoprecipitation for: 14-3-3, AKT, α-enolase, CHP1, HSP70 and HSP90. Additionally, we used The Cancer Genome Atlas (TCGA) to study NHE1 gene expression in primary patient breast tumours versus adjacent normal tissue. NHE1 expression was elevated in breast tumour samples and, when broken down by breast cancer subtype, NHE1 gene expression was significantly lower in tumours of the basal subtype compared to luminal and HER2 + subtypes. Reverse phase protein array (RPPA) analysis showed that NHE1 expression positively correlated with p90RSK expression in basal, but not luminal, primary tumours. Other proteins were negatively correlated with NHE1 expression in basal breast cancer tumours. Taken together, our data provides the first insight into the signalling molecules that form the NHE1 interactome in triple-negative breast cancer cells. These results will focus our search for novel targeted therapies.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cellular Signalling - Volume 29, January 2017, Pages 69-77
Journal: Cellular Signalling - Volume 29, January 2017, Pages 69-77
نویسندگان
Schammim Ray Amith, Krista Marie Vincent, Jodi Marie Wilkinson, Lynne Marie Postovit, Larry Fliegel,