Evidence map›Paper›PMID 28927124›Full record

ArticleOncology letters2017

Plasma membrane expression of ZNF185 is a prognostic factor in pancreatic ductal carcinoma.

Daisuke Furukawa, Tsuyoshi Chijiwa, Masahiro Matsuyama, Masaya Mukai, Ei-Ichi Matsuo, Osamu Nishimura, Kenji Kawai, Hiroshi Suemizu, Toshio Nakagohri, Soji Ozawa and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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 at 5 institutions in 1 country.

Daisuke FurukawaDivision of Pathology and Clinical Laboratories, National Cancer Center Research Institute, Tokyo 1040045, Japan.
Tsuyoshi ChijiwaCentral Institute for Experimental Animals, Kawasaki, Kanagawa 2100821, Japan.
Masahiro MatsuyamaDepartment of Surgery, Tokai University School of Medicine, Isehara, Kanagawa 2591193, Japan.
Masaya MukaiDepartment of Surgery, Tokai University Hachioji Hospital, Hachioji, Tokyo 1920032, Japan.
Ei-Ichi MatsuoGlobal Application Development Center, Shimadzu Corporation, Kyoto 6048511, Japan.
Osamu NishimuraInstitute for Protein Research, Osaka University, Suita, Osaka 5650871, Japan.
Kenji KawaiCentral Institute for Experimental Animals, Kawasaki, Kanagawa 2100821, Japan.
Hiroshi SuemizuCentral Institute for Experimental Animals, Kawasaki, Kanagawa 2100821, Japan.
Toshio NakagohriDepartment of Surgery, Tokai University School of Medicine, Isehara, Kanagawa 2591193, Japan.
Soji OzawaDepartment of Surgery, Tokai University School of Medicine, Isehara, Kanagawa 2591193, Japan.
Kazuaki ShimadaDivision of Hepatobiliary and Pancreatic Surgery, National Cancer Center Research Institute, Tokyo 1040045, Japan.
Nobuyoshi HiraokaDivision of Pathology and Clinical Laboratories, National Cancer Center Research Institute, Tokyo 1040045, Japan.
Masato NakamuraDepartment of Regenerative Medicine, Tokai University School of Medicine, Isehara, Kanagawa 2591193, Japan.
Tokai University · JPCentral Institute for Experimental Animals · JPOsaka University · JPShimadzu (Japan) · JPTokai University Hachioji Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal carcinoma (PDC) is one of the major causes of cancer-associated mortality globally due to its high potential for distant metastasis. To understand hematogenous metastasis, the molecular expression profiles of weak metastatic PDC cell subline BxPC-3 and highly liver-metastatic cell subline LM-BxPC-3 were compared, and zinc finger protein 185 (ZNF185) was identified as a molecule that is upregulated in LM-BxPC-3 cells. The aim of the present study was to evaluate the clinicopathological significance of ZNF185 in PDC. Using immunohistochemistry, ZNF185 expression was investigated in 182 patients with PDC, in association with numerous clinicopathological variables. The expression profile of ZNF185 was also characterized using xenograft models. In contrast to parent BxPC-3 cells in subcutaneous transplanted tumor foci, which only expressed ZNF185 on their plasma membrane (m)ZNF185, LM-BxPC-3 cells in liver-metastatic foci that were formed subsequent to transplantation all expressed cytoplasmic (c)ZNF185. Additionally, 51% of the cells at the periphery of the tumor foci expressed mZNF185. Expression of cZNF185, and of mZNF185 and cZNF185 combined was identified in 93 and 39% of clinical patients with PDC, respectively. Patients with mZNF185-negative and -positive PDC exhibited a median survival time of 30.2 months and 21.3 months, respectively. Multivariate analysis indicated that the expression of mZNF185 is closely associated with a shorter overall survival time. Increased marked venous invasion was more prevalent in patients who were mZNF185-positive, as compared with patients who were mZNF185-negative. These data suggest that the expression of mZNF185 is an independent and unfavorable prognosticator in patients with PDC. The results suggested that the amount and subcellular location of ZNF185 are correlated with the position of the cancer cells expressing it within the nests. Additionally, the subcellular location of ZNF185 may be important to its biological function.

Indexed as

hematogenous metastasispancreatic ductal carcinomaprognosissubcellular locationzinc finger protein 185

Identifiers

PMID28927124
PMCPMC5587964
OpenAlexW2738967563

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.