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High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma
BACKGROUND: Abnormal activation of the Sonic Hedgehog (SHH) signaling pathway contributing to carcinogenesis of some organs has been reported in the literature. We hypothesize that activation of the SHH pathway contributes to the recurrence of breast carcinoma. METHODS: Fifty consecutive patients wi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883580/ https://www.ncbi.nlm.nih.gov/pubmed/24403838 http://dx.doi.org/10.2147/OTT.S54702 |
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author | Jeng, Kuo-Shyang Sheen, I-Shyan Jeng, Wen-Juei Yu, Ming-Che Hsiau, Hsin-I Chang, Fang-Yu |
author_facet | Jeng, Kuo-Shyang Sheen, I-Shyan Jeng, Wen-Juei Yu, Ming-Che Hsiau, Hsin-I Chang, Fang-Yu |
author_sort | Jeng, Kuo-Shyang |
collection | PubMed |
description | BACKGROUND: Abnormal activation of the Sonic Hedgehog (SHH) signaling pathway contributing to carcinogenesis of some organs has been reported in the literature. We hypothesize that activation of the SHH pathway contributes to the recurrence of breast carcinoma. METHODS: Fifty consecutive patients with invasive breast carcinoma following curative resection were enrolled in this prospective study. The ratios of messenger RNA (mRNA) expression for Sonic Hedgehog (SHH), patched homolog-1 (PTCH-1), glioma-associated oncogene-1 (GLI-1), and smoothened (SMOH) were measured between breast carcinoma tissue and paired noncancerous breast tissue. These ratios were compared with their clinicopathologic characteristics. These factors and the mRNA ratios were compared between patients with recurrence and those without recurrence. RESULTS: The size of the invasive cancer correlated significantly with the ratio of SHH mRNA (P=0.001), that of PTCH-1 mRNA (P=0.005), and that of SMOH mRNA (P=0.021). Lymph node involvement correlated significantly with the ratio of SMOH mRNA (P=0.041). The correlation between Her-2 neu and the ratio of GLI-1 mRNA was statistically significant (P=0.012). Each ratio of mRNA of SHH, PTCH-1, GLI-1, and SMOH correlated significantly with cancer recurrence (P<0.001 for each). CONCLUSION: We suggest that high expression of SHH mRNA, PTCH-1 mRNA, GLI-1 mRNA, and SMOH mRNA in breast cancer tissue correlates with invasiveness and is a potential biomarker to predict postoperative recurrence. |
format | Online Article Text |
id | pubmed-3883580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38835802014-01-08 High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma Jeng, Kuo-Shyang Sheen, I-Shyan Jeng, Wen-Juei Yu, Ming-Che Hsiau, Hsin-I Chang, Fang-Yu Onco Targets Ther Original Research BACKGROUND: Abnormal activation of the Sonic Hedgehog (SHH) signaling pathway contributing to carcinogenesis of some organs has been reported in the literature. We hypothesize that activation of the SHH pathway contributes to the recurrence of breast carcinoma. METHODS: Fifty consecutive patients with invasive breast carcinoma following curative resection were enrolled in this prospective study. The ratios of messenger RNA (mRNA) expression for Sonic Hedgehog (SHH), patched homolog-1 (PTCH-1), glioma-associated oncogene-1 (GLI-1), and smoothened (SMOH) were measured between breast carcinoma tissue and paired noncancerous breast tissue. These ratios were compared with their clinicopathologic characteristics. These factors and the mRNA ratios were compared between patients with recurrence and those without recurrence. RESULTS: The size of the invasive cancer correlated significantly with the ratio of SHH mRNA (P=0.001), that of PTCH-1 mRNA (P=0.005), and that of SMOH mRNA (P=0.021). Lymph node involvement correlated significantly with the ratio of SMOH mRNA (P=0.041). The correlation between Her-2 neu and the ratio of GLI-1 mRNA was statistically significant (P=0.012). Each ratio of mRNA of SHH, PTCH-1, GLI-1, and SMOH correlated significantly with cancer recurrence (P<0.001 for each). CONCLUSION: We suggest that high expression of SHH mRNA, PTCH-1 mRNA, GLI-1 mRNA, and SMOH mRNA in breast cancer tissue correlates with invasiveness and is a potential biomarker to predict postoperative recurrence. Dove Medical Press 2013-12-27 /pmc/articles/PMC3883580/ /pubmed/24403838 http://dx.doi.org/10.2147/OTT.S54702 Text en © 2014 Jeng et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Jeng, Kuo-Shyang Sheen, I-Shyan Jeng, Wen-Juei Yu, Ming-Che Hsiau, Hsin-I Chang, Fang-Yu High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma |
title | High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma |
title_full | High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma |
title_fullStr | High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma |
title_full_unstemmed | High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma |
title_short | High expression of Sonic Hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma |
title_sort | high expression of sonic hedgehog signaling pathway genes indicates a risk of recurrence of breast carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883580/ https://www.ncbi.nlm.nih.gov/pubmed/24403838 http://dx.doi.org/10.2147/OTT.S54702 |
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