Evidence map›Paper›PMID 36018546›Full record

ArticleCancer science2022

Identification and validation of a poor clinical outcome subtype of primary prostate cancer with Midkine abundance.

Quan Zhou, Chen Yang, Zezhong Mou, Siqi Wu, Xiyu Dai, Xinan Chen, Yuxi Ou, Limin Zhang, Jianjun Sha, Haowen Jiang

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. RNA Interference based Midkine Gene Therapy for Hepatocellular Carcinoma.Asian Pacific journal of cancer prevention : APJCP · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. 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

10 authors at 2 institutions in 1 country.

Quan ZhouDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Chen YangDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Zezhong MouDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Siqi WuDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Xiyu DaiDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Xinan ChenDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Yuxi OuDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Limin ZhangDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Jianjun ShaDepartment of Urology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Haowen JiangDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.ORCID https://orcid.org/0000-0002-5349-1363
Fudan University · CNShanghai Jiao Tong University · CN

Funding

National Natural Science Foundation of China 81872102
6 · The paper itself

Abstract

Recent studies identified Midkine (MDK) as playing a key role in immune regulation. In this study, we aimed to discover the clinical significance and translational relevance in prostate cancer (PCa). We retrospectively analyzed 759 PCa patients who underwent radical prostatectomy from Huashan Hospital, Fudan University (training cohort, n = 369) and Chinese Prostate Cancer Consortium (validation cohort, n = 390). A total of 325 PCa patients from The Cancer Genome Atlas (TCGA) database (external cohort) were analyzed for exploration. Immune landscape and antitumor immunity were assessed through immunohistochemistry and flow cytometry. Patient-derived explant culture system was applied for evaluating the targeting potential of MDK. We found that intratumoral MDK expression correlated with PCa progression, which indicated an unfavorable biochemical recurrence (BCR)-free survival for postoperative PCa patients. Addition of MDK expression to the postoperative risk assessment tool CAPRA-S could improve its prognostic value. Tumors with MDK abundance characterized the tumor-infiltrating CD8

Indexed as

CD8-Positive T-LymphocytesProstatic NeoplasmsHumansMaleMidkinePrognosisRetrospective StudiesTumor MicroenvironmentMidkineadjuvant therapybiochemical recurrenceCD8+ T cellMidkineprostate cancer

Identifiers

PMID36018546
PMCPMC9633304
OpenAlexW4293125046

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.