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LIM only 4 is overexpressed in late stage pancreas cancer

BACKGROUND: LIM-only 4 (LMO4), a member of the LIM-only (LMO) subfamily of LIM domain-containing transcription factors, was initially reported to have an oncogenic role in breast cancer. We hypothesized that LMO4 may be related to pancreatic carcinogenesis as it is in breast carcinogenesis. If so, t...

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Autores principales: Yu, Jun, Ohuchida, Kenoki, Nakata, Kohei, Mizumoto, Kazuhiro, Cui, Lin, Fujita, Hayato, Yamaguchi, Hiroshi, Egami, Takuya, Kitada, Hidehisa, Tanaka, Masao
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628350/
https://www.ncbi.nlm.nih.gov/pubmed/19099607
http://dx.doi.org/10.1186/1476-4598-7-93
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author Yu, Jun
Ohuchida, Kenoki
Nakata, Kohei
Mizumoto, Kazuhiro
Cui, Lin
Fujita, Hayato
Yamaguchi, Hiroshi
Egami, Takuya
Kitada, Hidehisa
Tanaka, Masao
author_facet Yu, Jun
Ohuchida, Kenoki
Nakata, Kohei
Mizumoto, Kazuhiro
Cui, Lin
Fujita, Hayato
Yamaguchi, Hiroshi
Egami, Takuya
Kitada, Hidehisa
Tanaka, Masao
author_sort Yu, Jun
collection PubMed
description BACKGROUND: LIM-only 4 (LMO4), a member of the LIM-only (LMO) subfamily of LIM domain-containing transcription factors, was initially reported to have an oncogenic role in breast cancer. We hypothesized that LMO4 may be related to pancreatic carcinogenesis as it is in breast carcinogenesis. If so, this could result in a better understanding of tumorigenesis in pancreatic cancer. METHODS: We measured LMO4 mRNA levels in cultured cells, pancreatic bulk tissues and microdissected target cells (normal ductal cells; pancreatic intraepithelial neoplasia-1B [PanIN-1B] cells; PanIN-2 cells; invasive ductal carcinoma [IDC] cells; intraductal papillary-mucinous adenoma [IPMA] cells; IPM borderline [IPMB] cells; and invasive and non-invasive IPM carcinoma [IPMC]) by quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR). RESULTS: 9 of 14 pancreatic cancer cell lines expressed higher levels of LMO4 mRNA than did the human pancreatic ductal epithelial cell line (HPDE). In bulk tissue samples, expression of LMO4 was higher in pancreatic carcinoma than in intraductal papillary-mucinous neoplasm (IPMN) or non-neoplastic pancreas (p < 0.0001 for both). We carried out microdissection-based analyses. IDC cells expressed significantly higher levels of LMO4 than did normal ductal epithelia or PanIN-1B cells (p < 0.001 for both) or PanIN-2 cells (p = 0.014). IPMC cells expressed significantly higher levels of LMO4 than did normal ductal epithelia (p < 0.001), IPMA (p < 0.001) and IPMB cells (p = 0.003). CONCLUSION: Pancreatic carcinomas (both IDC and IPMC) expressed significantly higher levels of LMO4 mRNA than did normal ductal epithelia, PanIN-1B, PanIN-2, IPMA and IPMB. These results suggested that LMO4 is overexpressed at late stages in carcinogenesis of pancreatic cancer.
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spelling pubmed-26283502009-01-17 LIM only 4 is overexpressed in late stage pancreas cancer Yu, Jun Ohuchida, Kenoki Nakata, Kohei Mizumoto, Kazuhiro Cui, Lin Fujita, Hayato Yamaguchi, Hiroshi Egami, Takuya Kitada, Hidehisa Tanaka, Masao Mol Cancer Research BACKGROUND: LIM-only 4 (LMO4), a member of the LIM-only (LMO) subfamily of LIM domain-containing transcription factors, was initially reported to have an oncogenic role in breast cancer. We hypothesized that LMO4 may be related to pancreatic carcinogenesis as it is in breast carcinogenesis. If so, this could result in a better understanding of tumorigenesis in pancreatic cancer. METHODS: We measured LMO4 mRNA levels in cultured cells, pancreatic bulk tissues and microdissected target cells (normal ductal cells; pancreatic intraepithelial neoplasia-1B [PanIN-1B] cells; PanIN-2 cells; invasive ductal carcinoma [IDC] cells; intraductal papillary-mucinous adenoma [IPMA] cells; IPM borderline [IPMB] cells; and invasive and non-invasive IPM carcinoma [IPMC]) by quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR). RESULTS: 9 of 14 pancreatic cancer cell lines expressed higher levels of LMO4 mRNA than did the human pancreatic ductal epithelial cell line (HPDE). In bulk tissue samples, expression of LMO4 was higher in pancreatic carcinoma than in intraductal papillary-mucinous neoplasm (IPMN) or non-neoplastic pancreas (p < 0.0001 for both). We carried out microdissection-based analyses. IDC cells expressed significantly higher levels of LMO4 than did normal ductal epithelia or PanIN-1B cells (p < 0.001 for both) or PanIN-2 cells (p = 0.014). IPMC cells expressed significantly higher levels of LMO4 than did normal ductal epithelia (p < 0.001), IPMA (p < 0.001) and IPMB cells (p = 0.003). CONCLUSION: Pancreatic carcinomas (both IDC and IPMC) expressed significantly higher levels of LMO4 mRNA than did normal ductal epithelia, PanIN-1B, PanIN-2, IPMA and IPMB. These results suggested that LMO4 is overexpressed at late stages in carcinogenesis of pancreatic cancer. BioMed Central 2008-12-22 /pmc/articles/PMC2628350/ /pubmed/19099607 http://dx.doi.org/10.1186/1476-4598-7-93 Text en Copyright © 2008 Yu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Yu, Jun
Ohuchida, Kenoki
Nakata, Kohei
Mizumoto, Kazuhiro
Cui, Lin
Fujita, Hayato
Yamaguchi, Hiroshi
Egami, Takuya
Kitada, Hidehisa
Tanaka, Masao
LIM only 4 is overexpressed in late stage pancreas cancer
title LIM only 4 is overexpressed in late stage pancreas cancer
title_full LIM only 4 is overexpressed in late stage pancreas cancer
title_fullStr LIM only 4 is overexpressed in late stage pancreas cancer
title_full_unstemmed LIM only 4 is overexpressed in late stage pancreas cancer
title_short LIM only 4 is overexpressed in late stage pancreas cancer
title_sort lim only 4 is overexpressed in late stage pancreas cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628350/
https://www.ncbi.nlm.nih.gov/pubmed/19099607
http://dx.doi.org/10.1186/1476-4598-7-93
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