Expression of focal adhesion kinase gene and invasive cancer

T. M. Weiner; R. J. Craven; W. G. Cance; Et Liu

doi:10.1016/0140-6736(93)92881-S

Expression of focal adhesion kinase gene and invasive cancer

T. M. Weiner, R. J. Craven, W. G. Cance, Et Liu

Pharmacology and Nutritional Sciences

Research output: Contribution to journal › Article › peer-review

324 Scopus citations

Abstract

The focal adhesion kinase (FAK) gene produces a tyrosine kinase that localises to contact points between cells and extracellular matrix. It is believed to be an important signal molecule in cell adhesion. We have isolated a human homologue of the FAK gene from primary sarcomas and looked for FAK mRNA in 49 human tissue samples, including paired normal and neoplastic samples. We found increased levels of FAK in 1 of 8 adenomatous tissues, in 17 of 20 invasive tumours, and in all 15 metastatic tumours. There was no detectable FAK mRNA in 6 normal tissue samples. These observations suggest that FAK overexpression may accompany changes in signal pathways involved in tumour cell invasion. Lancet 1993; 342: 1024-25.

Original language	English
Pages (from-to)	1024-1025
Number of pages	2
Journal	The Lancet
Volume	342
Issue number	8878
DOIs	https://doi.org/10.1016/0140-6736(93)92881-S
State	Published - Oct 23 1993

Bibliographical note

Funding Information:
We thank Lori Kornberg and J Thomas Parsons for helpful discussions; and Jeanette Wedsworth for tumour procurement. This work is supported by National Cancer Institute grants K08-CA-01635 (WGC), 1-P50-CA- 58223-01 SPORE in breast cancer (ETL, RJC, WGC), Early Detection Research Network contract 5-3-35035 (WGC), T32 surgical oncology training grant CA-09688 (TMW), and American Cancer Society grant EDT-13A (ETL).

Funding Information:
We thank Mr Takao Souda for expert analytical assistance. This study was supported in part by research grants from the Morinaga Hoshikai, the Child Health Foundation, and the Mami Mizutani Foundation.

ASJC Scopus subject areas

General Medicine

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1016/0140-6736(93)92881-S

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title = "Expression of focal adhesion kinase gene and invasive cancer",

abstract = "The focal adhesion kinase (FAK) gene produces a tyrosine kinase that localises to contact points between cells and extracellular matrix. It is believed to be an important signal molecule in cell adhesion. We have isolated a human homologue of the FAK gene from primary sarcomas and looked for FAK mRNA in 49 human tissue samples, including paired normal and neoplastic samples. We found increased levels of FAK in 1 of 8 adenomatous tissues, in 17 of 20 invasive tumours, and in all 15 metastatic tumours. There was no detectable FAK mRNA in 6 normal tissue samples. These observations suggest that FAK overexpression may accompany changes in signal pathways involved in tumour cell invasion. Lancet 1993; 342: 1024-25.",

author = "Weiner, {T. M.} and Craven, {R. J.} and Cance, {W. G.} and Et Liu",

note = "Funding Information: We thank Lori Kornberg and J Thomas Parsons for helpful discussions; and Jeanette Wedsworth for tumour procurement. This work is supported by National Cancer Institute grants K08-CA-01635 (WGC), 1-P50-CA- 58223-01 SPORE in breast cancer (ETL, RJC, WGC), Early Detection Research Network contract 5-3-35035 (WGC), T32 surgical oncology training grant CA-09688 (TMW), and American Cancer Society grant EDT-13A (ETL). Funding Information: We thank Mr Takao Souda for expert analytical assistance. This study was supported in part by research grants from the Morinaga Hoshikai, the Child Health Foundation, and the Mami Mizutani Foundation.",

year = "1993",

month = oct,

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doi = "10.1016/0140-6736(93)92881-S",

language = "English",

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AU - Weiner, T. M.

AU - Craven, R. J.

AU - Cance, W. G.

AU - Liu, Et

N1 - Funding Information: We thank Lori Kornberg and J Thomas Parsons for helpful discussions; and Jeanette Wedsworth for tumour procurement. This work is supported by National Cancer Institute grants K08-CA-01635 (WGC), 1-P50-CA- 58223-01 SPORE in breast cancer (ETL, RJC, WGC), Early Detection Research Network contract 5-3-35035 (WGC), T32 surgical oncology training grant CA-09688 (TMW), and American Cancer Society grant EDT-13A (ETL). Funding Information: We thank Mr Takao Souda for expert analytical assistance. This study was supported in part by research grants from the Morinaga Hoshikai, the Child Health Foundation, and the Mami Mizutani Foundation.

PY - 1993/10/23

Y1 - 1993/10/23

N2 - The focal adhesion kinase (FAK) gene produces a tyrosine kinase that localises to contact points between cells and extracellular matrix. It is believed to be an important signal molecule in cell adhesion. We have isolated a human homologue of the FAK gene from primary sarcomas and looked for FAK mRNA in 49 human tissue samples, including paired normal and neoplastic samples. We found increased levels of FAK in 1 of 8 adenomatous tissues, in 17 of 20 invasive tumours, and in all 15 metastatic tumours. There was no detectable FAK mRNA in 6 normal tissue samples. These observations suggest that FAK overexpression may accompany changes in signal pathways involved in tumour cell invasion. Lancet 1993; 342: 1024-25.

AB - The focal adhesion kinase (FAK) gene produces a tyrosine kinase that localises to contact points between cells and extracellular matrix. It is believed to be an important signal molecule in cell adhesion. We have isolated a human homologue of the FAK gene from primary sarcomas and looked for FAK mRNA in 49 human tissue samples, including paired normal and neoplastic samples. We found increased levels of FAK in 1 of 8 adenomatous tissues, in 17 of 20 invasive tumours, and in all 15 metastatic tumours. There was no detectable FAK mRNA in 6 normal tissue samples. These observations suggest that FAK overexpression may accompany changes in signal pathways involved in tumour cell invasion. Lancet 1993; 342: 1024-25.

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JO - The Lancet

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Expression of focal adhesion kinase gene and invasive cancer

Abstract

Bibliographical note

ASJC Scopus subject areas

UN SDGs

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