Analysis of MUC6 polymorphisms on the clinicopathologic characteristics of Asian patients with oral squamous cell carcinoma
Head and neck squamous cell carcinomas (HNSCCs) are generally associated with tobacco consumption, alcohol abuse or both. Mucins (MUCs) are high‐molecular‐weight glycoproteins produced by many epithelial tissues. Many studies have indicated that MUCs play an important role in cancer metastasis. MUC6...
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Published in | Journal of cellular and molecular medicine Vol. 27; no. 17; pp. 2594 - 2602 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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England
John Wiley & Sons, Inc
01.09.2023
John Wiley and Sons Inc |
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Abstract | Head and neck squamous cell carcinomas (HNSCCs) are generally associated with tobacco consumption, alcohol abuse or both. Mucins (MUCs) are high‐molecular‐weight glycoproteins produced by many epithelial tissues. Many studies have indicated that MUCs play an important role in cancer metastasis. MUC6 expression has been observed in gastric and oncocytic phenotypes and plays an important role during cancer progression. We found that levels of MUC6 are lower in Asian HNCC patients and affect the disease‐free survival of HNCC patients. Next, we investigated the combined effect of MUC6 polymorphisms and exposure to environmental carcinogens on the susceptibility to and clinicopathological characteristics of HNCC. Three single‐nucleotide polymorphisms (SNPs) of MUC6 (rs7481521, rs6597947 and rs61869016) were analysed using real‐time PCR. After adjusting for other co‐variants, we found that carrying a CC genotype at MUC6 rs6597947 led to a lower risk of developing oral squamous cell carcinoma (OSCC) than wild‐type carriers among non‐betel‐quid chewers. Moreover, male oral cancer patients who carried the AA + CC genotype at MUC6 rs6597947 had a lower risk of lymph node metastasis than other genotypes, suggesting a significant functional compromise and decompensated disease. Therefore, our findings suggest that genetic variations in MUC6 may correlate to OSCC and indicate the progression in OSCC patients. |
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AbstractList | Head and neck squamous cell carcinomas (HNSCCs) are generally associated with tobacco consumption, alcohol abuse or both. Mucins (MUCs) are high-molecular-weight glycoproteins produced by many epithelial tissues. Many studies have indicated that MUCs play an important role in cancer metastasis. MUC6 expression has been observed in gastric and oncocytic phenotypes and plays an important role during cancer progression. We found that levels of MUC6 are lower in Asian HNCC patients and affect the disease-free survival of HNCC patients. Next, we investigated the combined effect of MUC6 polymorphisms and exposure to environmental carcinogens on the susceptibility to and clinicopathological characteristics of HNCC. Three single-nucleotide polymorphisms (SNPs) of MUC6 (rs7481521, rs6597947 and rs61869016) were analysed using real-time PCR. After adjusting for other co-variants, we found that carrying a CC genotype at MUC6 rs6597947 led to a lower risk of developing oral squamous cell carcinoma (OSCC) than wild-type carriers among non-betel-quid chewers. Moreover, male oral cancer patients who carried the AA + CC genotype at MUC6 rs6597947 had a lower risk of lymph node metastasis than other genotypes, suggesting a significant functional compromise and decompensated disease. Therefore, our findings suggest that genetic variations in MUC6 may correlate to OSCC and indicate the progression in OSCC patients.Head and neck squamous cell carcinomas (HNSCCs) are generally associated with tobacco consumption, alcohol abuse or both. Mucins (MUCs) are high-molecular-weight glycoproteins produced by many epithelial tissues. Many studies have indicated that MUCs play an important role in cancer metastasis. MUC6 expression has been observed in gastric and oncocytic phenotypes and plays an important role during cancer progression. We found that levels of MUC6 are lower in Asian HNCC patients and affect the disease-free survival of HNCC patients. Next, we investigated the combined effect of MUC6 polymorphisms and exposure to environmental carcinogens on the susceptibility to and clinicopathological characteristics of HNCC. Three single-nucleotide polymorphisms (SNPs) of MUC6 (rs7481521, rs6597947 and rs61869016) were analysed using real-time PCR. After adjusting for other co-variants, we found that carrying a CC genotype at MUC6 rs6597947 led to a lower risk of developing oral squamous cell carcinoma (OSCC) than wild-type carriers among non-betel-quid chewers. Moreover, male oral cancer patients who carried the AA + CC genotype at MUC6 rs6597947 had a lower risk of lymph node metastasis than other genotypes, suggesting a significant functional compromise and decompensated disease. Therefore, our findings suggest that genetic variations in MUC6 may correlate to OSCC and indicate the progression in OSCC patients. Head and neck squamous cell carcinomas (HNSCCs) are generally associated with tobacco consumption, alcohol abuse or both. Mucins (MUCs) are high-molecular-weight glycoproteins produced by many epithelial tissues. Many studies have indicated that MUCs play an important role in cancer metastasis. MUC6 expression has been observed in gastric and oncocytic phenotypes and plays an important role during cancer progression. We found that levels of MUC6 are lower in Asian HNCC patients and affect the disease-free survival of HNCC patients. Next, we investigated the combined effect of MUC6 polymorphisms and exposure to environmental carcinogens on the susceptibility to and clinicopathological characteristics of HNCC. Three single-nucleotide polymorphisms (SNPs) of MUC6 (rs7481521, rs6597947 and rs61869016) were analysed using real-time PCR. After adjusting for other co-variants, we found that carrying a CC genotype at MUC6 rs6597947 led to a lower risk of developing oral squamous cell carcinoma (OSCC) than wild-type carriers among non-betel-quid chewers. Moreover, male oral cancer patients who carried the AA + CC genotype at MUC6 rs6597947 had a lower risk of lymph node metastasis than other genotypes, suggesting a significant functional compromise and decompensated disease. Therefore, our findings suggest that genetic variations in MUC6 may correlate to OSCC and indicate the progression in OSCC patients. Head and neck squamous cell carcinomas (HNSCCs) are generally associated with tobacco consumption, alcohol abuse or both. Mucins (MUCs) are high‐molecular‐weight glycoproteins produced by many epithelial tissues. Many studies have indicated that MUCs play an important role in cancer metastasis. MUC6 expression has been observed in gastric and oncocytic phenotypes and plays an important role during cancer progression. We found that levels of MUC6 are lower in Asian HNCC patients and affect the disease‐free survival of HNCC patients. Next, we investigated the combined effect of MUC6 polymorphisms and exposure to environmental carcinogens on the susceptibility to and clinicopathological characteristics of HNCC. Three single‐nucleotide polymorphisms (SNPs) of MUC6 (rs7481521, rs6597947 and rs61869016) were analysed using real‐time PCR. After adjusting for other co‐variants, we found that carrying a CC genotype at MUC6 rs6597947 led to a lower risk of developing oral squamous cell carcinoma (OSCC) than wild‐type carriers among non‐betel‐quid chewers. Moreover, male oral cancer patients who carried the AA + CC genotype at MUC6 rs6597947 had a lower risk of lymph node metastasis than other genotypes, suggesting a significant functional compromise and decompensated disease. Therefore, our findings suggest that genetic variations in MUC6 may correlate to OSCC and indicate the progression in OSCC patients. |
Author | Chuang, Chun‐Yi Hua, Chun‐Hung Yang, Shun‐Fa Su, Chun‐Wen Yu, Yung‐Luen Chien, Yi‐Chung Chen, Shuo‐Chueh Liu, Liang‐Chih |
AuthorAffiliation | 7 Institute of Medicine Chung Shan Medical University Taichung Taiwan 4 Graduate Institute of Biomedical Sciences China Medical University Taichung Taiwan 10 School of Medicine, College of Medicine China Medical University Taichung Taiwan 8 Department of Medical Research Chung Shan Medical University Hospital Taichung Taiwan 9 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine China Medical University Hospital Taichung Taiwan 5 Institute of Translational Medicine and New Drug Development China Medical University Taichung Taiwan 6 Center for Molecular Medicine China Medical University Hospital Taichung Taiwan 3 Department of Otolaryngology Chung Shan Medical University Hospital Taichung Taiwan 1 Department of Otorhinolaryngology Head and Neck Surgery China Medical University Hospital Taichung Taiwan 11 Department of Surgery China Medical University Hospital Taichung Taiwan 12 Department of Medical Laboratory Science and Biotechnology Asia University Taichung Taiwan 2 |
AuthorAffiliation_xml | – name: 2 School of Medicine Chung Shan Medical University Taichung Taiwan – name: 3 Department of Otolaryngology Chung Shan Medical University Hospital Taichung Taiwan – name: 5 Institute of Translational Medicine and New Drug Development China Medical University Taichung Taiwan – name: 1 Department of Otorhinolaryngology Head and Neck Surgery China Medical University Hospital Taichung Taiwan – name: 11 Department of Surgery China Medical University Hospital Taichung Taiwan – name: 8 Department of Medical Research Chung Shan Medical University Hospital Taichung Taiwan – name: 4 Graduate Institute of Biomedical Sciences China Medical University Taichung Taiwan – name: 9 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine China Medical University Hospital Taichung Taiwan – name: 12 Department of Medical Laboratory Science and Biotechnology Asia University Taichung Taiwan – name: 6 Center for Molecular Medicine China Medical University Hospital Taichung Taiwan – name: 7 Institute of Medicine Chung Shan Medical University Taichung Taiwan – name: 10 School of Medicine, College of Medicine China Medical University Taichung Taiwan |
Author_xml | – sequence: 1 givenname: Chun‐Hung surname: Hua fullname: Hua, Chun‐Hung organization: China Medical University Hospital – sequence: 2 givenname: Chun‐Yi surname: Chuang fullname: Chuang, Chun‐Yi organization: Chung Shan Medical University Hospital – sequence: 3 givenname: Yi‐Chung surname: Chien fullname: Chien, Yi‐Chung organization: China Medical University Hospital – sequence: 4 givenname: Chun‐Wen surname: Su fullname: Su, Chun‐Wen organization: Chung Shan Medical University Hospital – sequence: 5 givenname: Shuo‐Chueh surname: Chen fullname: Chen, Shuo‐Chueh organization: China Medical University Hospital – sequence: 6 givenname: Liang‐Chih surname: Liu fullname: Liu, Liang‐Chih organization: China Medical University Hospital – sequence: 7 givenname: Shun‐Fa orcidid: 0000-0002-0365-7927 surname: Yang fullname: Yang, Shun‐Fa email: ysf@csmu.edu.tw organization: Chung Shan Medical University Hospital – sequence: 8 givenname: Yung‐Luen orcidid: 0000-0002-9745-1726 surname: Yu fullname: Yu, Yung‐Luen email: ylyu@mail.cmu.edu.tw organization: Asia University |
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Keywords | oral squamous cell carcinoma single-nucleotide polymorphisms MUC6 lymph node metastasis |
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SubjectTerms | Alcohol Alcohol abuse Carcinogens Drug abuse Genetic diversity Glycoproteins Head & neck cancer Head and neck carcinoma Liver cancer lymph node metastasis Lymph nodes Medical prognosis Metastases Metastasis MUC6 Mucin Oral cancer Oral carcinoma Oral squamous cell carcinoma Original Phenotypes Regression analysis Single-nucleotide polymorphism single‐nucleotide polymorphisms Smoking Software Squamous cell carcinoma |
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Title | Analysis of MUC6 polymorphisms on the clinicopathologic characteristics of Asian patients with oral squamous cell carcinoma |
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