Evidence map›Paper›PMID 25551773›Full record

ArticlePloS one2014

A comprehensive expression analysis of mucins in appendiceal carcinoma in a multicenter study: MUC3 is a novel prognostic factor.

Hiroaki Shibahara, Michiyo Higashi, Seiya Yokoyama, Karine Rousseau, Iwao Kitazono, Masahiko Osako, Hiroshi Shirahama, Yukie Tashiro, Yasuhiro Kurumiya, Michihiko Narita and 24 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  8. 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
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  15. Serum mucin 3A as a potential biomarker for extrahepatic cholangiocarcinoma.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association
    Article
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

34 authors at 20 institutions in 3 countries.

Hiroaki ShibaharaDepartment of Palliative Care, Toyota Kosei Hospital, Toyota, Japan.
Michiyo HigashiDepartment of Human Pathology, Field of Oncology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Seiya YokoyamaDepartment of Human Pathology, Field of Oncology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Karine RousseauWellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, United Kingdom.
Iwao KitazonoDepartment of Human Pathology, Field of Oncology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Masahiko OsakoDepartment of Surgery, Kagoshima Medical Association Hospital, Kagoshima, Japan.
Hiroshi ShirahamaDepartment of Pathology, Imakiire General Hospital, Kagoshima, Japan.
Yukie TashiroDepartment of Pathology, Imakiire General Hospital, Kagoshima, Japan.
Yasuhiro KurumiyaDepartment of Surgery, Toyota Kosei Hospital, Toyota, Japan.
Michihiko NaritaDepartment of Pathology, Toyota Kosei Hospital, Toyota, Japan.
Shingo KuzeDepartment of Surgery, Chutoen General Medical Center, Kakegawa, Japan.
Hiroshi HasagawaDepartment of Surgery, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.
Takehito KatoDepartment of Surgery, Toyohashi Municipal Hospital, Toyohashi, Japan.
Hitoshi KubotaDepartment of Surgery, Handa City Hospital, Handa, Japan.
Hideaki SuzukiDepartment of Surgery, Meijo Hospital, Nagoya, Japan.
Toshiyuki AraiDepartment of Surgery, Anjo Kosei Hospital, Anjo, Japan.
Yu SakaiDepartment of Pathology, Anjo Kosei Hospital, Anjo, Japan.
Norihiro YuasaDepartment of Surgery, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Japan.
Masahiko FujinoDepartment of Pathology, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Japan.
Shinji KondoDepartment of Surgery, Sakashita Hospital, Nakatsugawa, Japan.
Yoshichika OkamotoDepartment of Surgery, Shizuoka Saiseikai General Hospital, Shizuoka, Japan.
Tatsuyoshi YamamotoDepartment of Surgery, Tokai Hospital, Nagoya, Japan.
Takashi HiromatsuDepartment of Surgery, Kiryu Kosei General Hospital, Kiryu, Japan.
Eiji SasakiDepartment of Surgery, Kamiiida Daiichi General Hospital, Nagoya, Japan.
Kazuhisa ShiraiDepartment of Surgery, Yamashita Hospital, Ichinomiya, Japan.
Satoru KawaiDepartment of Surgery, Tsushima City Hospital, Tsushima, Japan.
Koutarou HattoriDepartment of Surgery, Minami Seikyo Hospital, Nagoya, Japan.
Hideki TsujiDepartment of Surgery, Toyota Memorial Hospital, Toyota, Japan.
Osamu OkochiDepartment of Surgery, Tosei General Hospital, Seto, Japan.
Masaki SakamotoDepartment of Surgery, Nagoya Tokushukai General Hospital, Kasugai, Japan.
Akinobu KondoDepartment of Surgery, Saiseikai Matsusaka General Hospital, Matsusaka, Japan.
Naomi KonishiDepartment of Surgery, Mie Prefectural General Medical Center, Yokkaichi, Japan.
Surinder K BatraDepartments of Biochemistry and Molecular Biology, Buffett Cancer Center, Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
Suguru YonezawaDepartment of Human Pathology, Field of Oncology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Kagoshima University · JPToyota Kosei Hospital · JPAnjo Kosei Hospital · JPImakiire General Hospital · JPJapanese Red Cross Nagoya Daiichi Hospital · JPHanda City Hospital · JPJapanese Red Cross Nagoya Daini Hospital · JPKagoshima Medical Center · JPKamiichi General Hospital · JPMatsunami General Hospital · JPMeijo Hospital · JPMie Chuo Medical Center · JPShizuoka Saiseikai General Hospital · JPTokai Central Hospital · JPTosei General Hospital · JPToyohashi Municipal Hospital · JPToyota Memorial Hospital · JPUniversity of Manchester · GBUniversity of Nebraska Medical Center · USYao Tokushukai General Hospital · JP

Funding

Role of N-Cadherin in Pancreatic Tumor MicroenvironmentU54CA163120 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLLINGSWORTH, MICHAEL A. · 2011 to 2015
$4.2M
NCI NIH HHS CA163120NCI NIH HHS U54 CA163120
6 · The paper itself

Abstract

backgroundMucins are implicated in survival in various cancers, but there have been no report addressed on survival in appendiceal carcinoma, an uncommon disease with different clinical and pathological features from those of other colon cancers. We aimed to investigate the clinical implications of expression of mucins in appendiceal carcinoma.

methodsExpression profiles of MUC1, MUC2, MUC3, MUC4, MUC5AC, MUC6, MUC16 and MUC17 in cancer tissue were examined by immunohistochemistry in 108 cases of surgically resected appendiceal carcinoma.

resultsThe following relationships of mucins with clinicopathologic factors were identified: MUC1 with positive lymphatic invasion (p = 0.036); MUC2 with histological type (mucinous carcinoma, p<0.001), superficial invasion depth (p = 0.007), negative venous invasion (p = 0.003), and curative resection (p = 0.019); MUC3 with non-curative resection (p = 0.017); MUC5AC with histological type (mucinous carcinoma, p = 0.002), negative lymphatic invasion (p = 0.021), and negative venous invasion (p = 0.022); and MUC16 with positive lymph node metastasis (p = 0.035), positive venous invasion (p<0.05), and non-curative resection (p = 0.035). A poor prognosis was related to positive lymph node metastasis (p = 0.04), positive lymphatic invasion (p = 0.02), positive venous invasion (p<0.001), non-curative resection (p<0.001), and positive expression of MUC3 (p = 0.004). In multivariate analysis, positive venous invasion (HR: 6.93, 95% CI: 1.93-24.96, p = 0.003), non-curative resection (HR: 10.19, 95% CI: 3.05-34.07, p<0.001) and positive MUC3 expression (HR: 3.37, 95% CI: 1.13-10.03, p = 0.03) were identified as significant independent prognostic factors in patients with appendiceal carcinoma.

conclusionsExpression of MUC3 in appendiceal carcinoma is an independent factor for poor prognosis and a useful predictor of outcome in patients with appendiceal carcinoma after surgery.

Indexed as

Gene Expression ProfilingAdultAgedAged, 80 and overAppendiceal NeoplasmsFemaleHumansMaleMiddle AgedMucinsMultivariate AnalysisPrognosisSurvival AnalysisYoung AdultMucins

Identifiers

PMID25551773
PMCPMC4281150
OpenAlexW1977079580

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.