Clinical Significance of GAB2, a Scaffolding/Docking Protein Acting Downstream of EGFR in Human Colorectal Cancer
Purpose Recent studies indicated that the scaffolding adaptor protein GAB2 (GRB2-associated binding protein 2) plays a critical role in the proliferation and migration of various cancers. This study aimed to determine the role of aberrant GAB2 expression in human colorectal cancer (CRC). Methods Qua...
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Veröffentlicht in: | Annals of surgical oncology 2014-12, Vol.21 (Suppl 4), p.743-749 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose
Recent studies indicated that the scaffolding adaptor protein GAB2 (GRB2-associated binding protein 2) plays a critical role in the proliferation and migration of various cancers. This study aimed to determine the role of aberrant
GAB2
expression in human colorectal cancer (CRC).
Methods
Quantitative real-time reverse transcription polymerase chain reaction was used to evaluate
GAB2
mRNA expression in 152 CRC tissues samples to determine the clinicopathological significance of
GAB2
expression. We also performed in vitro proliferation assays using si
GAB2
-transfected CRC cells.
Results
GAB2
expression in tumor colorectal tissues was significantly higher than in normal colorectal tissues (
p
= 0.0212). High
GAB2
expression levels were associated with malignant clinicopathologic potential factors, including lymphatic invasion (
p
= 0.0003), venous invasion (
p
= 0.0170), and liver metastasis (
p
= 0.0144). The survival rate of patients with high
GAB2
expression levels was significantly lower than that of patients with low
GAB2
expression (
p
= 0.0074). Multivariate analysis indicated that
GAB2
expression was a factor affecting lymph node metastasis. Cell proliferation was significantly suppressed by si
GAB2
expression in CRC cells in vitro.
Conclusions
GAB2
expression was associated with lymph node metastasis and may play a role in the growth and metastasis of CRC. These results suggest that
GAB2
is a potential therapeutic target in CRC. |
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ISSN: | 1068-9265 1534-4681 |
DOI: | 10.1245/s10434-014-3889-x |