Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical Cancer
Background: To investigate the diagnostic value of SMARCE1, cysteine-rich secreted protein 3 (CRISP3) combined with tumor markers in the diagnosis of cervical cancer. Methods: A total of 80 patients with cervical lesions who were diagnosed and treated in our hospital from January 2020 to March 2022...
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Format: | Article |
Language: | English |
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IMR Press
2023-02-01
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Series: | Clinical and Experimental Obstetrics & Gynecology |
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Online Access: | https://www.imrpress.com/journal/CEOG/50/2/10.31083/j.ceog5002045 |
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author | Lijie He Jing Wang Heping Zhang |
author_facet | Lijie He Jing Wang Heping Zhang |
author_sort | Lijie He |
collection | DOAJ |
description | Background: To investigate the diagnostic value of SMARCE1, cysteine-rich secreted protein 3 (CRISP3) combined with tumor markers in the diagnosis of cervical cancer. Methods: A total of 80 patients with cervical lesions who were diagnosed and treated in our hospital from January 2020 to March 2022 were selected and divided into control group (chronic cervicitis, n = 30) and observation group (cervical cancer, n = 50). Immunohistochemistry was used to detect the expression levels of SMARCE1 and CRISP3 in cervical tissue of the two groups of subjects, and the relationship between the expression of SMARCE1 and CRISP3 in cervical cancer tissue and the clinicopathological data of the patients was analyzed. In addition, the serum tumor marker levels of the two groups of subjects were detected, and the diagnostic value of SMARCE1 and CRISP3 combined with tumor markers in cervical cancer was analyzed. The female sexual function index (FSFI) and the functional assessment of cancer therapy-general (FACT-G) score were used to evaluate female sexual function and quality of life. Results: The positive expression rates of SMARCE1 and CRISP3 in the observation group were significantly higher than those in the control group (p < 0.05). There was no significant difference in the positive expression of SMARCE1 and CRISP3 among cervical cancer patients with age, lymph node metastasis and tumor node metastasis (TNM) classification stage (p > 0.05), and the lower the degree of tumor differentiation, the higher the positive expression rate of SMARCE1 and CRISP3 proteins (p < 0.05). The serum levels of carcinoembryonic antigen (CEA), carbohydrate antigen (CA) 125 and CA153 in the observation group were significantly higher than those in the control group (p < 0.05). The results of the receiver operating characteristic (ROC) curve analysis showed that the area under curve (AUC) values of SMARCE1, SMARCE1 + tumor markers, CRISP3, CRISP3 + tumor markers, SMARCE1, CRISP3 combined with tumor markers for the diagnosis of cervical cancer were 0.760, 0.851, 0.739, 0.810, and 0.944, respectively. Conclusions: SMARCE1 and CRISP3 are expressed in patients with cervical cancer, and CEA, CA125, and CA153 are expressed at high levels in the serum of patients with cervical cancer. The combined detection of SMARCE1 and CRISP3 combined with tumor markers has high clinical diagnostic value for cervical cancer. |
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institution | Directory Open Access Journal |
issn | 0390-6663 |
language | English |
last_indexed | 2024-04-10T06:49:02Z |
publishDate | 2023-02-01 |
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spelling | doaj.art-03978a4bce954943a96cede43ffed2aa2023-02-28T08:29:06ZengIMR PressClinical and Experimental Obstetrics & Gynecology0390-66632023-02-015024510.31083/j.ceog5002045S0390-6663(22)02001-2Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical CancerLijie He0Jing Wang1Heping Zhang2Department of Clinical Laboratory, Tianjin Fifth Central Hospital, 300450 Tianjin, ChinaDepartment of Clinical Laboratory, Tianjin Fifth Central Hospital, 300450 Tianjin, ChinaDepartment of Clinical Laboratory, Tianjin Fifth Central Hospital, 300450 Tianjin, ChinaBackground: To investigate the diagnostic value of SMARCE1, cysteine-rich secreted protein 3 (CRISP3) combined with tumor markers in the diagnosis of cervical cancer. Methods: A total of 80 patients with cervical lesions who were diagnosed and treated in our hospital from January 2020 to March 2022 were selected and divided into control group (chronic cervicitis, n = 30) and observation group (cervical cancer, n = 50). Immunohistochemistry was used to detect the expression levels of SMARCE1 and CRISP3 in cervical tissue of the two groups of subjects, and the relationship between the expression of SMARCE1 and CRISP3 in cervical cancer tissue and the clinicopathological data of the patients was analyzed. In addition, the serum tumor marker levels of the two groups of subjects were detected, and the diagnostic value of SMARCE1 and CRISP3 combined with tumor markers in cervical cancer was analyzed. The female sexual function index (FSFI) and the functional assessment of cancer therapy-general (FACT-G) score were used to evaluate female sexual function and quality of life. Results: The positive expression rates of SMARCE1 and CRISP3 in the observation group were significantly higher than those in the control group (p < 0.05). There was no significant difference in the positive expression of SMARCE1 and CRISP3 among cervical cancer patients with age, lymph node metastasis and tumor node metastasis (TNM) classification stage (p > 0.05), and the lower the degree of tumor differentiation, the higher the positive expression rate of SMARCE1 and CRISP3 proteins (p < 0.05). The serum levels of carcinoembryonic antigen (CEA), carbohydrate antigen (CA) 125 and CA153 in the observation group were significantly higher than those in the control group (p < 0.05). The results of the receiver operating characteristic (ROC) curve analysis showed that the area under curve (AUC) values of SMARCE1, SMARCE1 + tumor markers, CRISP3, CRISP3 + tumor markers, SMARCE1, CRISP3 combined with tumor markers for the diagnosis of cervical cancer were 0.760, 0.851, 0.739, 0.810, and 0.944, respectively. Conclusions: SMARCE1 and CRISP3 are expressed in patients with cervical cancer, and CEA, CA125, and CA153 are expressed at high levels in the serum of patients with cervical cancer. The combined detection of SMARCE1 and CRISP3 combined with tumor markers has high clinical diagnostic value for cervical cancer.https://www.imrpress.com/journal/CEOG/50/2/10.31083/j.ceog5002045smarce1crisp3tumor markerscervical cancerdiagnostic value |
spellingShingle | Lijie He Jing Wang Heping Zhang Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical Cancer Clinical and Experimental Obstetrics & Gynecology smarce1 crisp3 tumor markers cervical cancer diagnostic value |
title | Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical Cancer |
title_full | Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical Cancer |
title_fullStr | Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical Cancer |
title_full_unstemmed | Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical Cancer |
title_short | Diagnostic Value of SMARCE1 and CRISP3 Combined with Tumor Markers in Cervical Cancer |
title_sort | diagnostic value of smarce1 and crisp3 combined with tumor markers in cervical cancer |
topic | smarce1 crisp3 tumor markers cervical cancer diagnostic value |
url | https://www.imrpress.com/journal/CEOG/50/2/10.31083/j.ceog5002045 |
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