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INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance

BACKGROUND: Insulinoma-associated protein 1 (INSM1) has been identified as a nuclear marker of neuroendocrine tumors. Although INSM1 appears to be a subtle and specific biomarker for neuroendocrine tumor, its expression and clinicopathological significance in mesenchymal tumors remain unclear. METHO...

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Autores principales: Zhang, Qian, Dong, Yuting, Zhou, Meidong, Guo, Yujuan, Lou, Liping, Qu, Zhiling, Zheng, Yiyun, Duan, Yaqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750778/
https://www.ncbi.nlm.nih.gov/pubmed/36531655
http://dx.doi.org/10.1155/2022/1580410
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author Zhang, Qian
Dong, Yuting
Zhou, Meidong
Guo, Yujuan
Lou, Liping
Qu, Zhiling
Zheng, Yiyun
Duan, Yaqi
author_facet Zhang, Qian
Dong, Yuting
Zhou, Meidong
Guo, Yujuan
Lou, Liping
Qu, Zhiling
Zheng, Yiyun
Duan, Yaqi
author_sort Zhang, Qian
collection PubMed
description BACKGROUND: Insulinoma-associated protein 1 (INSM1) has been identified as a nuclear marker of neuroendocrine tumors. Although INSM1 appears to be a subtle and specific biomarker for neuroendocrine tumor, its expression and clinicopathological significance in mesenchymal tumors remain unclear. METHODS: We analyzed INSM1 mRNA level in GEO database and conducted immunohistological staining to detect the expression of INSM1 on 576 mesenchymal tumors from pathology department of Tongji Hospital. RESULTS: At transcription level, INSM1 expression in AITL (angioimmunoblastic T-cell lymphoma) was higher than their adjacent normal tissues as well as Hodgkin's lymphoma. Moreover, INSM1 expression in well-differentiated liposarcoma (WDLPS) was significantly higher than normal fat (P = 0.014) and dedifferentiated liposarcoma (DDLPS) (P = 0.0248). At protein level, the positive rate of INSM1 in AITL was 18/48 (47.4%), while in DDLPS was 9/20 (45%). INSM1 expression in AITL was significantly higher than Hodgkin's lymphoma (P = 0.008). And INSM1 expression in WDLPS was significantly lower than DDLPS (P = 0.015). CONCLUSION: The combination of GEO data and immunohistochemistry data indicated that the expression level of INSM1 was higher in AITL compared with normal control, suggesting that INSM1 may be involved in pathogenesis of AITL. The abnormal expression of INSM1 was found in WDLPS, and the positive rate of INSM1 was higher in DDLPS than in WDLPS. INSM1 may be involved in the regulation of liposarcoma development. There were significant differences in the expression of INSM1 between AITL and Hodgkin's lymphoma and WDLPS and DDLPS. These findings may assist in the differential diagnosis of these tumors when common markers are difficult to identify, enriching the diagnostic index system of mesenchymal tumors.
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spelling pubmed-97507782022-12-15 INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance Zhang, Qian Dong, Yuting Zhou, Meidong Guo, Yujuan Lou, Liping Qu, Zhiling Zheng, Yiyun Duan, Yaqi Biomed Res Int Research Article BACKGROUND: Insulinoma-associated protein 1 (INSM1) has been identified as a nuclear marker of neuroendocrine tumors. Although INSM1 appears to be a subtle and specific biomarker for neuroendocrine tumor, its expression and clinicopathological significance in mesenchymal tumors remain unclear. METHODS: We analyzed INSM1 mRNA level in GEO database and conducted immunohistological staining to detect the expression of INSM1 on 576 mesenchymal tumors from pathology department of Tongji Hospital. RESULTS: At transcription level, INSM1 expression in AITL (angioimmunoblastic T-cell lymphoma) was higher than their adjacent normal tissues as well as Hodgkin's lymphoma. Moreover, INSM1 expression in well-differentiated liposarcoma (WDLPS) was significantly higher than normal fat (P = 0.014) and dedifferentiated liposarcoma (DDLPS) (P = 0.0248). At protein level, the positive rate of INSM1 in AITL was 18/48 (47.4%), while in DDLPS was 9/20 (45%). INSM1 expression in AITL was significantly higher than Hodgkin's lymphoma (P = 0.008). And INSM1 expression in WDLPS was significantly lower than DDLPS (P = 0.015). CONCLUSION: The combination of GEO data and immunohistochemistry data indicated that the expression level of INSM1 was higher in AITL compared with normal control, suggesting that INSM1 may be involved in pathogenesis of AITL. The abnormal expression of INSM1 was found in WDLPS, and the positive rate of INSM1 was higher in DDLPS than in WDLPS. INSM1 may be involved in the regulation of liposarcoma development. There were significant differences in the expression of INSM1 between AITL and Hodgkin's lymphoma and WDLPS and DDLPS. These findings may assist in the differential diagnosis of these tumors when common markers are difficult to identify, enriching the diagnostic index system of mesenchymal tumors. Hindawi 2022-12-07 /pmc/articles/PMC9750778/ /pubmed/36531655 http://dx.doi.org/10.1155/2022/1580410 Text en Copyright © 2022 Qian Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Qian
Dong, Yuting
Zhou, Meidong
Guo, Yujuan
Lou, Liping
Qu, Zhiling
Zheng, Yiyun
Duan, Yaqi
INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance
title INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance
title_full INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance
title_fullStr INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance
title_full_unstemmed INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance
title_short INSM1 Expression in Mesenchymal Tumors and Its Clinicopathological Significance
title_sort insm1 expression in mesenchymal tumors and its clinicopathological significance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750778/
https://www.ncbi.nlm.nih.gov/pubmed/36531655
http://dx.doi.org/10.1155/2022/1580410
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