Evidence map›Paper›PMID 36209075›Full record

ArticleCellular & molecular biology letters2022

Exosomal DNAJB11 promotes the development of pancreatic cancer by modulating the EGFR/MAPK pathway.

Peng Liu, Fuqiang Zu, Hui Chen, Xiaoli Yin, Xiaodong Tan

Open access · goldAbstract read
In one paragraph

Article in Cellular & molecular biology letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Small extracellular vesicles (sEVs) in pancreatic cancer progression and diagnosis.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Exosomes: Emerging Insights into the Progression of Pancreatic Cancer.International journal of biological sciences · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
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

5 authors at 2 institutions in 1 country.

Peng LiuDepartment of General Surgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Fuqiang ZuDepartment of General Surgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Hui ChenDepartment of General Surgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Xiaoli Yin *Department of Radiology, Shengjing Hospital of China Medical University, Shenyang, 110004, China. yinxiaoli057728@163.com.
Xiaodong Tan *Department of General Surgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China. tanxdcmu@163.com.ORCID http://orcid.org/0000-0003-0862-1306
Shenyang Center for Disease Control and Prevention · CNChina Medical University · CN

Funding

Natural Science Foundation of Liaoning Province 180530068the Outstanding Young Doctor Fund of China Medical University QGZD2018050Young Scientists Fund 81902953
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a malignant tumor with invasive and metastatic characteristics and poor prognosis. Intracellular protein homeostasis is associated with invasion and metastasis of pancreatic cancer, but the specific molecular mechanism remains unclear. Our previous studies have revealed that DNAJB11, a key protein in protein homeostasis, is secreted by exosomes in the supernatant of dissociated pancreatic cancer cells with high metastasis. The results from transcriptome sequencing and co-immunoprecipitation (Co-IP)-based liquid chromatography with tandem mass spectrometry (LC-MS/MS) showed that depletion of DNAJB11 levels could increase HSPA5 expression and induce endoplasmic reticulum stress through the PRKR-like endoplasmic reticulum kinase signaling pathway in pancreatic cancer cells. Furthermore, exosomal DNAJB11 promoted cell development of PC cells in vitro and in vivo. In addition, exosomal DNAJB11 could regulate the expression of EGFR and activate the downstream MAPK signaling pathway. Clinical blood samples were collected to evaluate the potential of exosome DNAJB11 as a diagnostic biomarker and therapeutic target for the treatment of pancreatic cancer. This study could provide a new theoretical basis and potential molecular targets for the treatment of pancreatic cancer.

Indexed as

Pancreatic NeoplasmsTandem Mass SpectrometryAnimalsBiomarkersCell Line, TumorCell MovementCell ProliferationChromatography, LiquidErbB ReceptorsGene Expression Regulation, NeoplasticHSP40 Heat-Shock ProteinsHumansMAP Kinase Signaling SystemMiceMice, NudeBiomarkersDNAJB11 protein, humanEGFR protein, humanErbB ReceptorsHSP40 Heat-Shock ProteinsEarly diagnosisExosomal proteinPancreatic cancerSignal transduction

Identifiers

PMID36209075
PMCPMC9548179
OpenAlexW4303671949

What OpenQuestion holds

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LicenceCC BY
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.