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Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors

Mitotic counts in the World Health Organization (WHO) grading system have narrow cutoff values. True mitotic figures, however, are not always distinguishable from apoptotic bodies and darkly stained nuclei, complicating the ability of the WHO grading system to diagnose well-differentiated neuroendoc...

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Autores principales: Kim, Min Jeong, Kwon, Mi Jung, Kang, Ho Suk, Choi, Kyung Chan, Nam, Eun Sook, Cho, Seong Jin, Park, Hye-Rim, Min, Soo Kee, Seo, Jinwon, Choe, Ji-Young, Park, Hyoung-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892266/
https://www.ncbi.nlm.nih.gov/pubmed/29780816
http://dx.doi.org/10.1155/2018/1013640
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author Kim, Min Jeong
Kwon, Mi Jung
Kang, Ho Suk
Choi, Kyung Chan
Nam, Eun Sook
Cho, Seong Jin
Park, Hye-Rim
Min, Soo Kee
Seo, Jinwon
Choe, Ji-Young
Park, Hyoung-Chul
author_facet Kim, Min Jeong
Kwon, Mi Jung
Kang, Ho Suk
Choi, Kyung Chan
Nam, Eun Sook
Cho, Seong Jin
Park, Hye-Rim
Min, Soo Kee
Seo, Jinwon
Choe, Ji-Young
Park, Hyoung-Chul
author_sort Kim, Min Jeong
collection PubMed
description Mitotic counts in the World Health Organization (WHO) grading system have narrow cutoff values. True mitotic figures, however, are not always distinguishable from apoptotic bodies and darkly stained nuclei, complicating the ability of the WHO grading system to diagnose well-differentiated neuroendocrine tumors (NETs). The mitosis-specific marker phosphohistone H3 (PHH3) can identify true mitoses and grade tumors reliably. The aim of this study was to investigate the correspondence of tumor grades, as determined by PHH3 mitotic index (MI) and mitotic counts according to WHO criteria, and to determine the clinically relevant cutoffs of PHH3 MI in rectal and nonrectal gastrointestinal NETs. Mitotic counts correlated with both the Ki-67 labeling index and PHH3 MI, but the correlation with PHH3 MI was slightly higher. The PHH3 MI cutoff ≥4 correlated most closely with original WHO grades for both rectal NETs. A PHH3 MI cutoff ≥4, which could distinguish between G1 and G2 tumors, was associated with disease-free survival in patients with rectal NETs, whereas that cutoff value showed marginal significance for overall survival in patient with rectal NETs. In conclusion, the use of PHH3 ≥4 correlated most closely with original WHO grades.
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spelling pubmed-58922662018-05-20 Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors Kim, Min Jeong Kwon, Mi Jung Kang, Ho Suk Choi, Kyung Chan Nam, Eun Sook Cho, Seong Jin Park, Hye-Rim Min, Soo Kee Seo, Jinwon Choe, Ji-Young Park, Hyoung-Chul Biomed Res Int Research Article Mitotic counts in the World Health Organization (WHO) grading system have narrow cutoff values. True mitotic figures, however, are not always distinguishable from apoptotic bodies and darkly stained nuclei, complicating the ability of the WHO grading system to diagnose well-differentiated neuroendocrine tumors (NETs). The mitosis-specific marker phosphohistone H3 (PHH3) can identify true mitoses and grade tumors reliably. The aim of this study was to investigate the correspondence of tumor grades, as determined by PHH3 mitotic index (MI) and mitotic counts according to WHO criteria, and to determine the clinically relevant cutoffs of PHH3 MI in rectal and nonrectal gastrointestinal NETs. Mitotic counts correlated with both the Ki-67 labeling index and PHH3 MI, but the correlation with PHH3 MI was slightly higher. The PHH3 MI cutoff ≥4 correlated most closely with original WHO grades for both rectal NETs. A PHH3 MI cutoff ≥4, which could distinguish between G1 and G2 tumors, was associated with disease-free survival in patients with rectal NETs, whereas that cutoff value showed marginal significance for overall survival in patient with rectal NETs. In conclusion, the use of PHH3 ≥4 correlated most closely with original WHO grades. Hindawi 2018-03-27 /pmc/articles/PMC5892266/ /pubmed/29780816 http://dx.doi.org/10.1155/2018/1013640 Text en Copyright © 2018 Min Jeong Kim 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
Kim, Min Jeong
Kwon, Mi Jung
Kang, Ho Suk
Choi, Kyung Chan
Nam, Eun Sook
Cho, Seong Jin
Park, Hye-Rim
Min, Soo Kee
Seo, Jinwon
Choe, Ji-Young
Park, Hyoung-Chul
Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors
title Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors
title_full Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors
title_fullStr Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors
title_full_unstemmed Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors
title_short Identification of Phosphohistone H3 Cutoff Values Corresponding to Original WHO Grades but Distinguishable in Well-Differentiated Gastrointestinal Neuroendocrine Tumors
title_sort identification of phosphohistone h3 cutoff values corresponding to original who grades but distinguishable in well-differentiated gastrointestinal neuroendocrine tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892266/
https://www.ncbi.nlm.nih.gov/pubmed/29780816
http://dx.doi.org/10.1155/2018/1013640
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