Evidence map›Paper›PMID 34821375›Full record

ArticleHistology and histopathology2022

High Annexin A10 expression is correlated with poor prognosis in pancreatic ductal adenocarcinoma.

Akira Ishikawa, Kazuya Kuraoka, Junichi Zaitsu, Akihisa Saito, Atsushi Yamaguchi, Toshio Kuwai, Takeshi Sudo, Naoto Hadano, Hirotaka Tashiro, Kiyomi Taniyama and 1 more

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In one paragraph

Article in Histology and histopathology, 2022. 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
0.6field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Akira IshikawaInstitute for Clinical Laboratory, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Kazuya KuraokaInstitute for Clinical Laboratory, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan. kuraoka.kazuya.vk@mail.hosp.go.jp.
Junichi ZaitsuDepartment of Diagnostic Pathology, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Akihisa SaitoDepartment of Diagnostic Pathology, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Atsushi YamaguchiDepartment of Gastroenterology, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Toshio KuwaiDepartment of Gastroenterology, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Takeshi SudoDepartment of Surgery, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Naoto HadanoDepartment of Surgery, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Hirotaka TashiroDepartment of Surgery, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Kiyomi TaniyamaHonorary President, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Aoyama, Kure, Japan.
Wataru YasuifDepartment of Molecular Pathology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Kasumi, Minami-ku, Hiroshima, Japan.
Kure Medical Center · JPHiroshima University · JP

Funding

KAKENHI Grant in Aid for Early-Career Scientists, Japan Society for the Promotion of Science JP21K15394
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is the third-leading cause of cancer-related death. Owing to its poor prognosis, new molecular biomarkers for PDAC are needed. Annexin A10 (ANXA10) is a calcium-/phospholipid-binding protein belonging to the annexin family of proteins. ANXA10 is not only associated with gastric phenotypes, but also acts an independent prognostic factor in several cancers. However, the role of ANXA10 in PDAC remains unknown. Therefore, we examined the relationship between ANXA10 and the prognosis of PDAC. We analyzed the expression of ANXA10 using data from public databases, and performed immunohistochemistry analysis for 81 PDAC cases. We then investigated the relationship between ANXA10 expression and clinicopathological features. ANXA10 was detected in 47 of 81 PDAC cases (58%). High expression of ANXA10 was significantly related to poor overall survival (OS; p=0.011). Univariate analysis of OS revealed three prognostic parameters: tumor grade (p=0.046), perineural invasion (p=0.017), and ANXA10 expression (p=0.012). Multivariate analysis indicated that ANXA10 expression (p<0.01) alone was a prognostic factor in PDAC cases. Our findings suggest that ANXA10 expression is an independent prognostic factor in PDAC cases and shows promise as a new biomarker in PDAC.

Indexed as

AnnexinsCarcinoma, Pancreatic DuctalPancreatic NeoplasmsBiomarkers, TumorHumansPrognosisAnnexinsANXA10 protein, humanBiomarkers, Tumor

Identifiers

PMID34821375
OpenAlexW3215930945

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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.