Evidence map›Paper›PMID 26759717›Full record

ArticleGigaScience2016

Genomic analyses reveal FAM84B and the NOTCH pathway are associated with the progression of esophageal squamous cell carcinoma.

Caixia Cheng, Heyang Cui, Ling Zhang, Zhiwu Jia, Bin Song, Fang Wang, Yaoping Li, Jing Liu, Pengzhou Kong, Ruyi Shi and 23 more

Open access · goldAbstract read
In one paragraph

Article in GigaScience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 4% of its field
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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Pooled it
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  12. Study Deciphering the Crucial Involvement of Notch Signaling Pathway in Human Cancers.Endocrine, metabolic & immune disorders drug targets · 2024
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  14. Roles of oncogenes in esophageal squamous cell carcinoma and their therapeutic potentials.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  15. Review
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  20. An in vitro vesicle formation assay reveals cargo clients and factors that mediate vesicular trafficking.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

33 authors at 6 institutions in 1 country.

Caixia ChengTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Department of Pathology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Heyang CuiTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Ling ZhangTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Zhiwu JiaTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Bin SongTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Department of Oncology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Fang WangTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Yaoping LiTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Department of Tumor Surgery, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Jing LiuTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Department of General Surgery, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Pengzhou KongTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Ruyi ShiTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Yanghui BiTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Bin YangTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Department of Tumor Surgery, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Juan WangTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Zhenxiang ZhaoTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Yanyan ZhangTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Department of General Surgery, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Xiaoling HuTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Jie YangTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Chanting HeTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Zhiping ZhaoTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Jinfen WangDepartment of Pathology, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Yanfeng XiDepartment of Pathology, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Enwei XuDepartment of Pathology, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Guodong LiDepartment of Pathology, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Shiping GuoDepartment of Tumor Surgery, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Yunqing ChenDepartment of Tumor Surgery, Shanxi Cancer Hospital, Taiyuan, Shanxi 030001 China.
Xiaofeng YangDepartment of Urology Surgery, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Xing ChenDepartment of Endoscopy, Shanxi Provincial People's Hospital, Taiyuan, Shanxi 030001 China.
Jianfang LiangDepartment of Pathology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Jiansheng GuoDepartment of General Surgery, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Xiaolong ChengTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Chuangui WangInstitute of Translational Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 201620 China.
Qimin ZhanCancer Institute and Cancer Hospital, State Key Laboratory of Molecular Oncology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021 China.
Yongping CuiTranslational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001 China ; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001 China.
Shanxi Medical University · CNShanxi Provincial Cancer Hospital · CNFirst Hospital of Shanxi Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNShaanxi Provincial People's Hospital · CNShanghai First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEsophageal squamous cell carcinoma (ESCC) is the sixth most lethal cancer worldwide and the fourth most lethal cancer in China. Genomic characterization of tumors, particularly those of different stages, is likely to reveal additional oncogenic mechanisms. Although copy number alterations and somatic point mutations associated with the development of ESCC have been identified by array-based technologies and genome-wide studies, the genomic characterization of ESCCs from different stages of the disease has not been explored. Here, we have performed either whole-genome sequencing or whole-exome sequencing on 51 stage I and 53 stage III ESCC patients to characterize the genomic alterations that occur during the various clinical stages of ESCC, and further validated these changes in 36 atypical hyperplasia samples.

resultsRecurrent somatic amplifications at 8q were found to be enriched in stage I tumors and the deletions of 4p-q and 5q were particularly identified in stage III tumors. In particular, the FAM84B gene was amplified and overexpressed in preclinical and ESCC tumors. Knockdown of FAM84B in ESCC cell lines significantly reduced in vitro cell growth, migration and invasion. Although the cancer-associated genes TP53, PIK3CA, CDKN2A and their pathways showed no significant difference between stage I and stage III tumors, we identified and validated a prevalence of mutations in NOTCH1 and in the NOTCH pathway that indicate that they are involved in the preclinical and early stages of ESCC.

conclusionsOur results suggest that FAM84B and the NOTCH pathway are involved in the progression of ESCC and may be potential diagnostic targets for ESCC susceptibility.

Indexed as

AdultAgedCarcinoma, Squamous CellCell Line, TumorCell MovementChromosome DeletionDisease ProgressionDNA Copy Number VariationsEsophageal NeoplasmsGenetic Predisposition to DiseaseGenome, HumanHumansImmunohistochemistryIn Situ Hybridization, FluorescenceMaleMembrane ProteinsLRATD2 protein, humanMembrane ProteinsNeoplasm ProteinsReceptors, NotchESCCFAM84BNext-generation sequencingNOTCH signaling

Identifiers

PMID26759717
PMCPMC4709967
OpenAlexW2237089710

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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.