Reach Us +44-1647-403003
Tackling Cellular Hierarchies In Cancer: Transcriptional And Epigenetic Regulation Of Stem Cells In Myeloid Leukemias As A Paradigm | 5166
ISSN: 2157-7013

Journal of Cell Science & Therapy
Open Access

Like us on:

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Tackling cellular hierarchies in cancer: Transcriptional and epigenetic regulation of stem cells in myeloid leukemias as a paradigm

International Conference & Exhibition on Cell Science & Stem Cell Research

Ulrich G. Steidl

ScientificTracks Abstracts: J Cell Sci Ther

DOI: 10.4172/2157-7013.S1.02

Due to its invasive nature, glioblastoma (GBM) is the most aggressive brain cancer. Hepatocyte growth factor (HGF) binds to MET tyrosine kinase receptor and induces invasive tumor growth. As MET inhibitors are entering clinical trials against several types of cancer including GBM, it is compelling to identify therapeutic determinants which could indicate which patient subsets are suitable for this therapy. We investigated in vivo three types of GBM models for their sensitivity to MET or EGFR inhibitors: 1) Tumors sustained by an HGF- autocrine loop; 2) tumors displaying paracrine HGF tumor growth; and 3) tumors with MET polysomy and EGFR amplifi cationOf the three tumor types, we observed that HGF- autocrine activation correlates with p-MET levels in the HGF autocrine GBM cell lines, which in turn are extremely sensitive to MET inhibition in vivo . Moreover, serum HGF levels in HGF-autocrine loop GBM xenograft s correlate with MET inhibition. Paracrine HGF can enhance GBM growth in vivo , but they were not signifi cantly sensitive to MET inhibition. In type three tumors, EGFR VIII amplifi cation predicted sensitivity to erlotinib, but MET polysomy in the same tumor did not display MET activity and the cells did not show sensitivity to MET inhibition. We conclude that HGF- autocrine activation GBM tumors bear an activated MET signaling pathway that may be used to predict sensitivity to MET inhibitors in GBM patients. However, targeting MET alone may not be suffi cient for treating GBM and the combination of MET with other RTK inhibitors, especially EGFR inhibitors should be considered
Dr. Xie completed her doctorate in Oncology from Fudan University in China. She then joined the Laboratory of Molecular Oncology (LMO) at Van Andel Research Institute as a postdoctoral fellow. She has been continuously working on the MET signaling pathway, focusing mainly on brain cancer. Dr. Xie is currently a Senior Research Scientist in the (LMO) under the direction of Dr. George Vande Woude; her major research goal is to understand the mechanism of brain cancer malignancy and to develop novel strategies particular with MET inhibitors to target glioblastoma.
Relevant Topics