Evidence map›Paper›PMID 29780816›Full record

ArticleBioMed research international2018

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

Min Jeong Kim, Mi Jung Kwon, Ho Suk Kang, Kyung Chan Choi, Eun Sook Nam, Seong Jin Cho, Hye-Rim Park, Soo Kee Min, Jinwon Seo, Ji-Young Choe and 1 more

Abstract read
In one paragraph

Article in BioMed research international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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  3. Different miRNAs Related toInternational journal of molecular sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Min Jeong KimDepartment of Surgery, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, 150 Seongan-ro, Gangdong-gu, Seoul 05355, Republic of Korea.
Mi Jung KwonDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, 170beon-gil, 22 Gwanpyeong-ro, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Republic of Korea.ORCID 0000-0002-2441-0448
Ho Suk KangDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, 170beon-gil, 22 Gwanpyeong-ro, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Republic of Korea.
Kyung Chan ChoiDepartment of Pathology, Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Chuncheon, Republic of Korea.
Eun Sook NamDepartment of Pathology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, 150 Seongan-ro, Gangdong-gu, Seoul 05355, Republic of Korea.
Seong Jin ChoDepartment of Pathology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, 150 Seongan-ro, Gangdong-gu, Seoul 05355, Republic of Korea.
Hye-Rim ParkDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, 170beon-gil, 22 Gwanpyeong-ro, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Republic of Korea.
Soo Kee MinDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, 170beon-gil, 22 Gwanpyeong-ro, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Republic of Korea.ORCID 0000-0002-7099-9433
Jinwon SeoDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, 170beon-gil, 22 Gwanpyeong-ro, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Republic of Korea.
Ji-Young ChoeDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, 170beon-gil, 22 Gwanpyeong-ro, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Republic of Korea.
Hyoung-Chul ParkDepartment of Surgery, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, 170beon-gil, 22 Gwanpyeong-ro, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Republic of Korea.ORCID 0000-0002-1369-8757

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AdolescentAdultAgedAged, 80 and overBiomarkers, TumorChildDisease-Free SurvivalFemaleGastrointestinal NeoplasmsHistonesHumansKi-67 AntigenMaleMiddle AgedMitosisMitotic IndexBiomarkers, TumorHistonesKi-67 Antigen

Identifiers

PMID29780816
PMCPMC5892266

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.