Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2008-7-18
pubmed:abstractText
Signaling downstream of Ras is mediated by three major pathways, Raf/ERK, phosphatidylinositol 3 kinase (PI3K), and Ral guanine nucleotide exchange factor (RalGEF). Ras signal transduction pathways play an important role in breast cancer progression, as evidenced by the frequent over-expression of the Ras-activating epidermal growth factor receptors EGFR and ErbB2. Here we investigated which signal transduction pathways downstream of Ras contribute to EGFR-dependent transformation of telomerase-immortalized mammary epithelial cells HME16C. Furthermore, we examined whether a highly transcriptionally regulated ERK pathway target, PHLDA1 (TDAG51), suggested to be a tumor suppressor in breast cancer and melanoma, might modulate the transformation process.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-10428057, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-10440377, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-10594239, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-10956414, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-10998351, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-11316792, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-11333208, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-11369516, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-11467446, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-11790801, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-11823860, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-12183360, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-12384558, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-12738777, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-12781366, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-12944910, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-14709771, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-15037619, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-15090615, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-15143186, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-15254419, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-15324700, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-15480434, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-17024176, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-17211533, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-17575221, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-17692807, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-17699800, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-17709381, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-2547513, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-3798106, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-7867061, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-8066447, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-8463179, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-8673705, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-9362489, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-9751783, http://linkedlifedata.com/resource/pubmed/commentcorrection/18597688-9811723
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1471-2407
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
8
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
189
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
TDAG51 is an ERK signaling target that opposes ERK-mediated HME16C mammary epithelial cell transformation.
pubmed:affiliation
Cell and Cancer Biology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 37 Convent Drive, Room 1066, Bethesda, MD 20892, USA. michaeloberst@gmail.com
pubmed:publicationType
Journal Article, Research Support, N.I.H., Intramural