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Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study
The Journal of pathology, 2012-09, Vol.228 (1), p.119-130
Gadd, Samantha
Beezhold, Patricia
Jennings, Lawrence
George, David
Leuer, Katrin
Huang, Chiang-Ching
Huff, Vicki
Tognon, Cristina
Sorensen, Poul HB
Triche, Timothy
Coffin, Cheryl M
Perlman, Elizabeth J
2012
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Gadd, Samantha
Beezhold, Patricia
Jennings, Lawrence
George, David
Leuer, Katrin
Huang, Chiang-Ching
Huff, Vicki
Tognon, Cristina
Sorensen, Poul HB
Triche, Timothy
Coffin, Cheryl M
Perlman, Elizabeth J
Titel
Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study
Ist Teil von
The Journal of pathology, 2012-09, Vol.228 (1), p.119-130
Ort / Verlag
Chichester, UK: John Wiley & Sons, Ltd
Erscheinungsjahr
2012
Quelle
MEDLINE
Beschreibungen/Notizen
Infantile fibrosarcoma (IFS; also known as cellular congenital mesoblastic nephroma, CMN, when in the kidney) is a rare, undifferentiated tumour often characterized by the ETV6‐NTRK3 fusion transcript. Our goal was to identify downstream pathways, diagnostic markers and potential therapeutic targets for IFS/CMN. Global gene expression, reverse‐phase protein array and ETV6‐NTRK3 fusion analyses were performed on 14 IFS/CMN and compared with 41 other paediatric renal tumours. These analyses confirm significant receptor tyrosine kinase (RTK) activation, with evidence of PI3‐Akt, MAPK and SRC activation. In particular, GAB2 docking protein, STAT5‐pTyr‐694, STAT3‐pSer‐729 and YAP‐pSer‐127 were elevated, and TAZ‐pSer‐89 was decreased. This provides mRNA and proteomic evidence that GAB2, STAT activation and phosphorylation of the Hippo pathway transcription co‐activators YAP and TAZ contribute to the RTK signal transduction in IFS/CMN. All IFS/CMN tumours displayed a distinctive gene expression pattern that may be diagnostically useful. Unexpectedly, abundant ETV6‐NTRK3 transcript copies were present in only 7/14 IFS, with very low copy number in 3/14. An additional 4/14 were negative by RT‐PCR and absence of ETV6‐NTRK3 was confirmed by FISH for both ETV6 and NTRK3. Therefore, molecular mechanisms other than ETV6‐NTRK3 fusion are responsible for the development of some IFS/CMNs and the absence of ETV6‐NTRK3 fusion products should not exclude IFS/CMN as a diagnosis. Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
Sprache
Englisch
Identifikatoren
ISSN: 0022-3417
eISSN: 1096-9896
DOI: 10.1002/path.4010
Titel-ID: cdi_proquest_miscellaneous_1030502417
Format
–
Schlagworte
Biological and medical sciences
,
Biomarkers, Tumor - metabolism
,
congenital fibrosarcoma
,
DNA, Neoplasm - analysis
,
ETS Translocation Variant 6 Protein
,
ETV6-NTRK3
,
GAB2
,
Gene Expression Regulation, Neoplastic - physiology
,
Hippo
,
Humans
,
In Situ Hybridization, Fluorescence
,
infantile fibrosarcoma
,
Investigative techniques, diagnostic techniques (general aspects)
,
Kidney Neoplasms - genetics
,
Kidney Neoplasms - metabolism
,
Kidneys
,
Medical sciences
,
mesoblastic nephroma
,
Mitogen-Activated Protein Kinase Kinases - metabolism
,
Nephrology. Urinary tract diseases
,
Nephroma, Mesoblastic - genetics
,
Nephroma, Mesoblastic - metabolism
,
Oncogene Proteins, Fusion - genetics
,
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
,
Phosphatidylinositol 3-Kinases - metabolism
,
Proto-Oncogene Proteins c-ets - genetics
,
Proto-Oncogene Proteins c-ets - metabolism
,
Proto-Oncogene Proteins pp60(c-src) - metabolism
,
Receptor, trkC - genetics
,
Receptor, trkC - metabolism
,
Repressor Proteins - genetics
,
Repressor Proteins - metabolism
,
Tumors of the urinary system
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