SUOX is negatively associated with multistep carcinogenesis and proliferation in oral squamous cell carcinoma
Oral squamous cell carcinoma (OSCC) is the most common malignant tumor in the head and neck region. The aim of this study was to identify the key molecules and to elucidate the molecular mechanisms of OSCC carcinogenesis through a microarray analysis of RNA extracted from normal epithelium, dysplasi...
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| Published in | Medical molecular morphology Vol. 51; no. 2; pp. 102 - 110 |
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| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Tokyo
Springer Japan
01.06.2018
Springer Nature B.V |
| Subjects | |
| Online Access | Get full text |
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| Abstract | Oral squamous cell carcinoma (OSCC) is the most common malignant tumor in the head and neck region. The aim of this study was to identify the key molecules and to elucidate the molecular mechanisms of OSCC carcinogenesis through a microarray analysis of RNA extracted from normal epithelium, dysplasia, and squamous cell carcinoma components. Out of molecules that showed changes in gene expression in the microarray analysis, we focused on Sulfite oxidase (SUOX), which correlated significantly with carcinogenic process and exhibited a stepwise decrease in expression. The expression of SUOX was evaluated in detail at the protein level using samples from 58 patients with cancer of the tongue, and correlating clinicopathological factors were also comprehensively examined. SUOX expression declined significantly from normal epithelium to dysplasia to squamous cell carcinoma components in line with carcinogenic process. With regard to squamous cell carcinoma, SUOX expression was significantly lower when T classification was high. Our findings indicated that SUOX is negatively associated with the progression and proliferation of tongue cancer, and suggest that SUOX may be a key molecule in tongue tumors. |
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| AbstractList | Oral squamous cell carcinoma (OSCC) is the most common malignant tumor in the head and neck region. The aim of this study was to identify the key molecules and to elucidate the molecular mechanisms of OSCC carcinogenesis through a microarray analysis of RNA extracted from normal epithelium, dysplasia, and squamous cell carcinoma components. Out of molecules that showed changes in gene expression in the microarray analysis, we focused on Sulfite oxidase (SUOX), which correlated significantly with carcinogenic process and exhibited a stepwise decrease in expression. The expression of SUOX was evaluated in detail at the protein level using samples from 58 patients with cancer of the tongue, and correlating clinicopathological factors were also comprehensively examined. SUOX expression declined significantly from normal epithelium to dysplasia to squamous cell carcinoma components in line with carcinogenic process. With regard to squamous cell carcinoma, SUOX expression was significantly lower when T classification was high. Our findings indicated that SUOX is negatively associated with the progression and proliferation of tongue cancer, and suggest that SUOX may be a key molecule in tongue tumors. |
| Author | Akiba, Jun Ogasawara, Sachiko Naito, Yoshiki Nakayama, Masamichi Kusukawa, Jingo Abe, Yushi Nakamura, Ken Yano, Hirohisa |
| Author_xml | – sequence: 1 givenname: Ken surname: Nakamura fullname: Nakamura, Ken organization: Department of Pathology, Kurume University School of Medicine, Dental and Oral Medical Center, Kurume University School of Medicine – sequence: 2 givenname: Jun surname: Akiba fullname: Akiba, Jun email: akiba@med.kurume-u.ac.jp organization: Department of Pathology, Kurume University School of Medicine, Department of Diagnostic Pathology, Kurume University Hospital – sequence: 3 givenname: Sachiko surname: Ogasawara fullname: Ogasawara, Sachiko organization: Department of Pathology, Kurume University School of Medicine – sequence: 4 givenname: Yoshiki surname: Naito fullname: Naito, Yoshiki organization: Department of Diagnostic Pathology, Kurume University Hospital – sequence: 5 givenname: Masamichi surname: Nakayama fullname: Nakayama, Masamichi organization: Department of Pathology, Kurume University School of Medicine – sequence: 6 givenname: Yushi surname: Abe fullname: Abe, Yushi organization: Department of Pathology, Kurume University School of Medicine, Dental and Oral Medical Center, Kurume University School of Medicine – sequence: 7 givenname: Jingo surname: Kusukawa fullname: Kusukawa, Jingo organization: Dental and Oral Medical Center, Kurume University School of Medicine – sequence: 8 givenname: Hirohisa surname: Yano fullname: Yano, Hirohisa organization: Department of Pathology, Kurume University School of Medicine |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29280012$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_3389_fmicb_2024_1310444 crossref_primary_10_1007_s00795_018_00214_1 crossref_primary_10_1007_s10142_020_00738_9 crossref_primary_10_1016_j_ecoenv_2024_116617 crossref_primary_10_1016_j_humpath_2022_06_020 crossref_primary_10_3390_ijms22126506 crossref_primary_10_3892_ol_2021_12974 crossref_primary_10_1111_jcmm_14344 crossref_primary_10_1111_hepr_13365 |
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| Copyright | The Japanese Society for Clinical Molecular Morphology 2017 Medical Molecular Morphology is a copyright of Springer, (2017). All Rights Reserved. |
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| Keywords | Immunohistochemistry Dysplasia Oral squamous cell carcinoma Sulfite oxidase Microarray Carcinogenesis |
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| Snippet | Oral squamous cell carcinoma (OSCC) is the most common malignant tumor in the head and neck region. The aim of this study was to identify the key molecules and... |
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| StartPage | 102 |
| SubjectTerms | Anatomy Carcinogenesis DNA microarrays Dysplasia Epithelium Gene expression Medicine Medicine & Public Health Molecular Medicine Molecular modelling Neck Oral cancer Oral squamous cell carcinoma Original Paper Pathology Ribonucleic acid RNA Squamous cell carcinoma Sulfite Sulfite oxidase Tongue Tumors |
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| Title | SUOX is negatively associated with multistep carcinogenesis and proliferation in oral squamous cell carcinoma |
| URI | https://link.springer.com/article/10.1007/s00795-017-0177-4 https://www.ncbi.nlm.nih.gov/pubmed/29280012 https://www.proquest.com/docview/1980689624 |
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