Evidence map›Paper›PMID 34895266›Full record

ArticleDiagnostic pathology2021

Clinicopathological and molecular genomic features of monomorphic epitheliotropic intestinal T-cell lymphoma in the Chinese population: a study of 20 cases.

Chunni Chen, Yuxi Gong, Yefan Yang, Qiuyuan Xia, Qiu Rao, Yang Shao, Liuqing Zhu, Junli Zhang, Xiao Li, Pan Ji and 3 more

Abstract read
In one paragraph

Article in Diagnostic pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

13 authors.

Chunni Chen *Department of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China.
Yuxi Gong *Department of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China.
Yefan YangDepartment of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China.
Qiuyuan XiaDepartment of Pathology, Nanjing Jinling Hospital, Nanjing University School of Medicine, 210002, Nanjing, Jiangsu Province, China.
Qiu RaoDepartment of Pathology, Nanjing Jinling Hospital, Nanjing University School of Medicine, 210002, Nanjing, Jiangsu Province, China.
Yang ShaoNanjing Geneseeq Technology Inc, 210032, Nanjing, Jiangsu Province, China.
Liuqing ZhuNanjing Geneseeq Technology Inc, 210032, Nanjing, Jiangsu Province, China.
Junli ZhangNanjing Geneseeq Technology Inc, 210032, Nanjing, Jiangsu Province, China.
Xiao LiDepartment of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China.
Pan JiDepartment of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China.
Boya ZhaiDepartment of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China.
Xiang ZhangDepartment of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China.
Zhihong ZhangDepartment of Pathology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, 210029, Nanjing, Jiangsu Province, China. zhangzh@njmu.edu.cn.

Funding

Fund of the priority Academic Program Development of Jiangsu Higher Education Institution JX1023-1801Joint key project funded by Southeast University and Nanjing Medical University 2242019K3DN09, JX218GSP20190735National key Clinical Specialty Construction Project 2014National Natural Science Foundation of China 81773109Natural Science Foundation of Jiangsu Province BK20151582
6 · The paper itself

Abstract

backgroundMonomorphic epitheliotropic T-cell lymphoma (MEITL) is an aggressive non-Hodgkin lymphoma with a high fatality rate. This study was aimed to explore the clinicopathological and molecular genetic features of MEITL in the Chinese population.

methodsA retrospective analysis was performed based on the clinical manifestations and pathological features of 20 Chinese MEITL. 9 cases with paired diseased-normal tissues were also analyzed for molecular information by whole-exome sequencing.

resultsThere were 14 men and 6 women with a median age of 58.5 (28-81) years. 17(17/20) lesions were located in the jejunum or ileum; 13(13/20) cases had ulcers or perforations. Microscopically, except for 1(1/20) case of pleomorphic cells, the monomorphic, middle-sized tumor cells infiltrating into the intestinal epithelial and peripheral intestinal mucosa recess could be seen in the other 19 cases. Immunohistochemistry showed that most of the tumor cells in MEITL were positive for CD3(20/20), CD8(17/20), CD43(19/20), and CD56(15/20), but negative for CD5(20/20). The most frequently mutated genes of these Chinese cases were STAT5B (4/9) and TP53 (4/9), not SETD2(2/9). JAK3 mutations (3/9) were also detected with a high mutated frequency. We demonstrated that mutations of JAK-STAT pathway-related genes and the amplification of Chromosome 9q appeared at the same time in most cases(5/9).

conclusionsThe clinicopathological features were consistent with that in previous western studies, but a special case with pleomorphic cells was found in this study. The co-occurrence of JAK-STAT pathway-related gene mutations and the amplification of Chr9q is a molecular feature of MEITL.

Indexed as

Chromosomes, Human, Pair 9Gene AmplificationMutationAdultAgedAged, 80 and overBiomarkers, TumorChinaDNA Mutational AnalysisExome SequencingFemaleGenetic Predisposition to DiseaseHumansIntestinal NeoplasmsJanus Kinase 3Lymphoma, T-CellBiomarkers, TumorJAK3 protein, humanJanus Kinase 3STAT5B protein, humanSTAT5 Transcription FactorAmplification of chromosome 9qJAK-STAT pathwayMonomorphic epitheliotropic intestinal T-cell lymphomaWhole-exome sequencing

Identifiers

PMID34895266
PMCPMC8667391

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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.