Evidence map›Paper›PMID 41976399›Full record

ArticleCancers2026

Comparison of Comprehensive Serum miRNA Sequencing and Apolipoprotein A2 Isoforms for Early Detection of Pancreatic Cancer.

Hirotaka Kashima, Munenori Kawai, Kei Iimori, Munemasa Nagao, Takamitsu J Morikawa, Ryo Otomo, Mitsuharu Hirai, Kosuke Minaga, Masanori Asada, Atsushi Umemura and 16 more

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

26 authors.

Hirotaka KashimaDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0009-0003-1701-9672
Munenori KawaiDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0000-0001-9784-1487
Kei IimoriDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0009-0006-7420-1173
Munemasa NagaoDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0000-0003-0789-6623
Takamitsu J MorikawaResearch and Development Division, ARKRAY, Inc., Yousuien-nai, 59 Gansuin-cho, Kamigyo-ku, Kyoto 606-8507, Japan.
Ryo OtomoResearch and Development Division, ARKRAY, Inc., Yousuien-nai, 59 Gansuin-cho, Kamigyo-ku, Kyoto 606-8507, Japan.
Mitsuharu HiraiResearch and Development Division, ARKRAY, Inc., Yousuien-nai, 59 Gansuin-cho, Kamigyo-ku, Kyoto 606-8507, Japan.ORCID 0000-0002-7633-9161
Kosuke MinagaDepartment of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka 589-8511, Japan.
Masanori AsadaDepartment of Gastroenterology and Hepatology, Japanese Red Cross Osaka Hospital, Osaka 543-8555, Japan.ORCID 0000-0002-7478-7649
Atsushi UmemuraDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Yoshito UenoyamaDepartment of Gastroenterology and Hepatology, Japanese Red Cross Wakayama Medical Center, Wakayama 640-8558, Japan.
Toshihiro MoritaDepartment of Gastroenterology and Hepatology, Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka 530-8480, Japan.ORCID 0000-0002-4114-9894
Shujiro YazumiDepartment of Gastroenterology and Hepatology, Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka 530-8480, Japan.ORCID 0000-0002-0683-0000
Ryuki MinamiDepartment of Gastroenterology, Tenri Hospital, Nara 632-0032, Japan.
Saiko MaruiDepartment of Gastroenterology and Hepatology, Shiga General Hospital, Moriyama 524-8524, Japan.
Yuki YamauchiDepartment of Gastroenterology, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki 661-0892, Japan.
Yoshitaka NakaiDepartment of Gastroenterology and Hepatology, Kyoto Katsura Hospital, Kyoto 615-8256, Japan.
Yutaka TakadaDepartment of Gastroenterology and Hepatology, Kobe City Nishi-Kobe Medical Center, Kobe 651-2273, Japan.
Seiji ShioDivision of Gastroenterology, Shinko Hospital, Kobe 651-0072, Japan.
Takuto YoshiokaDepartment of Gastroenterology and Hepatology, Takatsuki Red Cross Hospital, Takatsuki 569-1096, Japan.ORCID 0000-0003-1097-6632
Naoki KandaDepartment of Gastroenterology and Hepatology, Takatsuki Red Cross Hospital, Takatsuki 569-1096, Japan.
Tomonori MasudaDepartment of Gastroenterology and Hepatology, Japanese Red Cross Otsu Hospital, Otsu 520-0046, Japan.ORCID 0000-0002-1967-5644
Kazuyuki NagaiDivision of Hepato-Biliary-Pancreatic Surgery and Transplantation, Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan.
Etsuro HatanoDivision of Hepato-Biliary-Pancreatic Surgery and Transplantation, Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan.
Akihisa FukudaDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0000-0002-1940-596X
Hiroshi SenoDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

Funding

Arkray (Japan) N/A
6 · The paper itself

Abstract

BACKGROUNDS AND

aimPancreatic cancer is frequently diagnosed at advanced stages, highlighting the need for biomarkers that are capable of detecting early-stage disease in asymptomatic individuals. Recently, apolipoprotein A2 isoforms (ApoA2-ATQ/AT) have been reported as a new blood biomarker for pancreatic cancer. We recently developed diagnostic models based on 100 highly expressed serum microRNAs (miRNAs) combined with CA19-9; these models achieved high accuracy in terms of distinguishing individuals with pancreatic cancer from healthy individuals. This study aimed to compare the diagnostic performance of these miRNA-based models with that of the ApoA2-ATQ/AT biomarker.

methodsComprehensive sequencing of serum miRNAs was conducted using samples from 120 pancreatic cancer patients recruited across 14 hospitals, along with 93 healthy controls without cancer. Serum CA19-9 levels, miRNA index values, miRNA+CA19-9 index values, and ApoA2 index values were assessed. miRNA-based indices were derived from classification models built on an automated machine-learning platform.

resultsThe miRNA model (AUC 0.94; 95% CI 0.91-0.97) and the miRNA+CA19-9 model (AUC 0.99; 95% CI 0.98-1.00) outperformed ApoA2 (AUC 0.89; 95% CI 0.84-0.93) in terms of distinguishing individuals with pancreatic cancer from healthy controls across all stages. In early-stage disease (stages 0-I and 0-II), both miRNA-based models also demonstrated superior performance. Strong negative correlations were observed between the ApoA2 index and both the miRNA model index (r = -0.62) and the miRNA+CA19-9 index (r = -0.63).

conclusionsThese findings suggest that miRNA-based diagnostic models, particularly when combined with CA19-9, could serve as powerful tools for the early detection of pancreatic cancer.

Indexed as

APOA2 isoformCA19-9miRNANGSpancreatic cancer

Identifiers

PMID41976399
PMCPMC13072215

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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.