Evidence map›Paper›PMID 35633503›Full record

ArticleCancer science2022

Prosaposin, tumor-secreted protein, promotes pancreatic cancer progression by decreasing tumor-infiltrating lymphocytes.

Yoji Miyahara, Shigetsugu Takano, Kazuyuki Sogawa, Satoshi Tomizawa, Katsunori Furukawa, Tsukasa Takayashiki, Satoshi Kuboki, Masayuki Ohtsuka

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. 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
1.4field-weighted citation impact, top 20% 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, 17 citations in OpenAlex.

  1. Review
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  11. The Multifaced Role of Collagen in Cancer Development and Progression.International journal of molecular sciences · 2024
    Review
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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

8 authors at 2 institutions in 1 country.

Yoji MiyaharaDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID https://orcid.org/0000-0001-5636-2607
Shigetsugu TakanoDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID https://orcid.org/0000-0002-6495-0422
Kazuyuki SogawaDepartment of Biochemistry, School of Life and Environmental Science, Azabu University, Kanagawa, Japan.
Satoshi TomizawaDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Katsunori FurukawaDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Tsukasa TakayashikiDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Satoshi KubokiDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Masayuki OhtsukaDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Chiba University · JPAzabu University · JP

Funding

Grant-in-Aid for Scientific Research (KAKENHI) 19H03725Grant-in-Aid for Scientific Research (KAKENHI) 19K09113
6 · The paper itself

Abstract

Glycoproteins produced by tumor cells are involved in cancer progression, metastasis, and the immune response, and serve as possible therapeutic targets. Considering the dismal outcomes of pancreatic ductal adenocarcinoma (PDAC) due to its unique tumor microenvironment, which is characterized by low antitumor T-cell infiltration, we hypothesized that tumor-derived glycoproteins may serve as regulating the tumor microenvironment. We used glycoproteomics with tandem mass tag labeling to investigate the culture media of three human PDAC cell lines, and attempted to identify the key secreted proteins from PDAC cells. Among the identified glycoproteins, prosaposin (PSAP) was investigated for its functional contribution to PDAC progression. PSAP is highly expressed in various PDAC cell lines; however, knockdown of intrinsic PSAP expression did not affect the proliferation and migration capacities. Based on the immunohistochemistry of resected human PDAC tissues, high PSAP expression was associated with poor prognosis in patients with PDAC. Notably, tumors with high PSAP expression showed significantly lower CD8

Indexed as

Carcinoma, Pancreatic DuctalLymphocytes, Tumor-InfiltratingPancreatic NeoplasmsSaposinsCD8-Positive T-LymphocytesCell Line, TumorHumansRNA, Small InterferingTumor MicroenvironmentPSAP protein, humanRNA, Small InterferingSaposinsantitumor immunitypancreatic ductal adenocarcinomaprosaposintumor-infiltrating lymphocytestumor microenvironment

Identifiers

PMID35633503
PMCPMC9357616
OpenAlexW4281678407

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.