Evidence map›Paper›PMID 28349447›Full record

ArticleInternational urology and nephrology2017

Overexpression of placenta specific 8 is associated with malignant progression and poor prognosis of clear cell renal cell carcinoma.

Liping Shi, Long Xiao, Baoli Heng, Shijie Mo, Weijun Chen, Zexuan Su

Abstract read
PubMed Publisher
In one paragraph

Article in International urology and nephrology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Novel Prognostic Markers for Skin Cutaneous Melanoma.Clinical, cosmetic and investigational dermatology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Multifaced roles of PLAC8 in cancer.Biomarker research · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

6 authors at 1 institution in 1 country.

Liping ShiDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, China.
Long XiaoDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, China.
Baoli HengDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, China.
Shijie MoDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, China.
Weijun ChenDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, China.
Zexuan SuDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, China. bolyheng@126.com.
First Affiliated Hospital of Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlacenta specific 8 (PLAC8) plays an important role in many different cellular processes and human diseases, including multiple types of cancer. However, the functional role of PLAC8 in clear cell renal cell carcinoma (ccRCC) has never been elucidated.

methodsPLAC8 mRNA expression was investigated in 31 pairs of fresh ccRCC tumor tissues and matched adjacent non-tumor tissues by RT-qPCR and confirmed by analyzing the TCGA KRCC dataset which contains RNA-seq data of 534 ccRCC and 72 solid normal tissues. Protein level of PLAC8 expression was also investigated using immunohistochemistry in 129 ccRCC samples. Correlations with clinicopathological factors and overall survival were analyzed. To examine its effect on the biological activity, PLAC8 siRNAs were transfected into ccRCC cells. Cell proliferation was assessed by CCK8 cell viability assays, clone formation assays, and EdU incorporation assays. Cell invasion was examined using transwell assays. RNA sequencing was then performed to further elucidate the mechanisms by which PLAC8 regulates the cancer.

resultsPLAC8 expression was positively correlated with tumor size, metastasis, and clinical stage of ccRCC. Additionally, high PLAC8 expression was closely associated with a shorter overall survival time. Knockdown of PLAC8 with siRNAs significantly reduced the proliferation and invasion of RCC cells and increased the sensitivity of RCC cells to cisplatin. RNA-seq analysis revealed that knockdown of PLAC8 down-regulated the expression of a panel of inflammatory mediators, which suggested that PLAC8 is associated with the ccRCC inflammatory microenvironment. Patients with high expression of PLAC8 had a significantly higher number of infiltrative lymphocytes than patients with low expression of PLAC8.

conclusionOur findings suggest that PLAC8 may be a potential prognostic indicator and therapeutic target for ccRCC.

Indexed as

Antineoplastic AgentsCarcinoma, Renal CellCell Line, TumorCell ProliferationCisplatinDisease ProgressionDrug Resistance, NeoplasmFemaleGene ExpressionGene Expression Regulation, NeoplasticHumansInflammationKidneyKidney NeoplasmsLymphocytes, Tumor-InfiltratingMaleAntineoplastic AgentsCisplatinPLAC8 protein, humanProteinsRNA, MessengerRNA, Small InterferingCell proliferationInflammatoryInvasionPLAC8PrognosisRenal cell carcinoma

Identifiers

PMID28349447
OpenAlexW2599509028

What OpenQuestion holds

Textmetadata
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.