Truncated ErbB2 receptor enhances ErbB1 signaling and induces reversible, ERK‐independent loss of epithelial morphology

Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH2‐terminally truncated ErbB2 correlates with lymph node metastases and adverse outcome in human breast cancer. To study the possible signaling from such a truncated receptor, MCF‐7 human brea...

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Published inInternational journal of cancer Vol. 94; no. 2; pp. 185 - 191
Main Authors Egeblad, Mikala, Mortensen, Ole H., Jäättelä, Marja
Format Journal Article
LanguageEnglish
Published New York John Wiley & Sons, Inc 15.10.2001
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Abstract Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH2‐terminally truncated ErbB2 correlates with lymph node metastases and adverse outcome in human breast cancer. To study the possible signaling from such a truncated receptor, MCF‐7 human breast cancer cells expressing NH2‐terminally truncated ErbB2 (ΔNErbB2) were compared with cells overexpressing wild‐type ErbB2. Expression of ΔNErbB2 in MCF‐7 cells resulted in sustained activation of extracellular signal‐regulated kinases (ERK) 1/2, extensive loss of the epithelial morphology, appearance of vesicles and long protrusions as well as pronounced scattering of the cells. Similar alterations were observed upon ErbB2 overexpression but at much lower levels. Employing cell clones with inducible expression of ΔNErbB2, it was revealed that the morphological changes were fully reversible and depended on continuous expression of ΔNErbB2 but not on the activation of the ERK1/2 pathway. Interestingly, the expression of ΔNErbB2 resulted also in the increased expression and phosphorylation of ErbB1 as well as in the prolonged ligand‐induced activation of the ErbB1 signaling pathway. In conclusion, constitutive signaling upon expression of the truncated ErbB2 receptor in human breast cancer cells promotes morphological changes indicative of a more motile and aggressive phenotype. © 2001 Wiley‐Liss, Inc.
AbstractList Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH(2)-terminally truncated ErbB2 correlates with lymph node metastases and adverse outcome in human breast cancer. To study the possible signaling from such a truncated receptor, MCF-7 human breast cancer cells expressing NH(2)-terminally truncated ErbB2 (DeltaNErbB2) were compared with cells overexpressing wild-type ErbB2. Expression of DeltaNErbB2 in MCF-7 cells resulted in sustained activation of extracellular signal-regulated kinases (ERK) 1/2, extensive loss of the epithelial morphology, appearance of vesicles and long protrusions as well as pronounced scattering of the cells. Similar alterations were observed upon ErbB2 overexpression but at much lower levels. Employing cell clones with inducible expression of DeltaNErbB2, it was revealed that the morphological changes were fully reversible and depended on continuous expression of DeltaNErbB2 but not on the activation of the ERK1/2 pathway. Interestingly, the expression of DeltaNErbB2 resulted also in the increased expression and phosphorylation of ErbB1 as well as in the prolonged ligand-induced activation of the ErbB1 signaling pathway. In conclusion, constitutive signaling upon expression of the truncated ErbB2 receptor in human breast cancer cells promotes morphological changes indicative of a more motile and aggressive phenotype.
Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH sub(2)-terminally truncated ErbB2 correlates with lymph node metastases and adverse outcome in human breast cancer. To study the possible signaling from such a truncated receptor, MCF-7 human breast cancer cells expressing NH sub(2)-terminally truncated ErbB2 ( Delta NErbB2) were compared with cells overexpressing wild-type ErbB2. Expression of Delta NErbB2 in MCF-7 cells resulted in sustained activation of extracellular signal-regulated kinases (ERK) 1/2, extensive loss of the epithelial morphology, appearance of vesicles and long protrusions as well as pronounced scattering of the cells. Similar alterations were observed upon ErbB2 overexpression but at much lower levels. Employing cell clones with inducible expression of Delta NErbB2, it was revealed that the morphological changes were fully reversible and depended on continuous expression of Delta NErbB2 but not on the activation of the ERK1/2 pathway. Interestingly, the expression of Delta NErbB2 resulted also in the increased expression and phosphorylation of ErbB 1 as well as in the prolonged ligand-induced activation of the ErbB1 signaling pathway. In conclusion, constitutive signaling upon expression of the truncated ErbB2 receptor in human breast cancer cells promotes morphological changes indicative of a more motile and aggressive phenotype.
Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH2‐terminally truncated ErbB2 correlates with lymph node metastases and adverse outcome in human breast cancer. To study the possible signaling from such a truncated receptor, MCF‐7 human breast cancer cells expressing NH2‐terminally truncated ErbB2 (ΔNErbB2) were compared with cells overexpressing wild‐type ErbB2. Expression of ΔNErbB2 in MCF‐7 cells resulted in sustained activation of extracellular signal‐regulated kinases (ERK) 1/2, extensive loss of the epithelial morphology, appearance of vesicles and long protrusions as well as pronounced scattering of the cells. Similar alterations were observed upon ErbB2 overexpression but at much lower levels. Employing cell clones with inducible expression of ΔNErbB2, it was revealed that the morphological changes were fully reversible and depended on continuous expression of ΔNErbB2 but not on the activation of the ERK1/2 pathway. Interestingly, the expression of ΔNErbB2 resulted also in the increased expression and phosphorylation of ErbB1 as well as in the prolonged ligand‐induced activation of the ErbB1 signaling pathway. In conclusion, constitutive signaling upon expression of the truncated ErbB2 receptor in human breast cancer cells promotes morphological changes indicative of a more motile and aggressive phenotype. © 2001 Wiley‐Liss, Inc.
Author Egeblad, Mikala
Jäättelä, Marja
Mortensen, Ole H.
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Snippet Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH2‐terminally truncated ErbB2 correlates with lymph...
Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH(2)-terminally truncated ErbB2 correlates with...
Shedding of the extracellular domain of the ErbB2 tyrosine kinase receptor and expression of the remaining NH sub(2)-terminally truncated ErbB2 correlates with...
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StartPage 185
SubjectTerms Breast Neoplasms - pathology
EGFR
Enzyme Activation
Epidermal Growth Factor - pharmacology
Epithelial Cells - pathology
ErbB Receptors - physiology
ErbB2
ErbB2 protein
ERK protein
Female
Humans
MAP kinase
Mitogen-Activated Protein Kinases - physiology
morphology
Receptor, ErbB-2 - chemistry
Receptor, ErbB-2 - physiology
Tumor Cells, Cultured
Title Truncated ErbB2 receptor enhances ErbB1 signaling and induces reversible, ERK‐independent loss of epithelial morphology
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fijc.1459
https://www.ncbi.nlm.nih.gov/pubmed/11668496
https://search.proquest.com/docview/18188641
https://search.proquest.com/docview/72222589
Volume 94
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