Evidence map›Paper›PMID 24696714›Full record

ArticleInternational journal of clinical and experimental pathology2014

HLJ1 is a novel biomarker for colorectal carcinoma progression and overall patient survival.

Yong Liu, Jie Zhou, Cuiwei Zhang, Wenguang Fu, Xiuli Xiao, Sibei Ruan, Yuan Zhang, Xia Luo, Mingxi Tang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.5field-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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The role of HSP40 in cancer: Recent advances.Histology and histopathology · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Genetic Deletion of HLJ1 Does Not Affect Blood Coagulation in Mice.International journal of molecular sciences · 2022
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. HLJ1 (DNAJB4) Gene Is a Novel Biomarker Candidate in Breast Cancer.Omics : a journal of integrative biology · 2017
    Article
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Yong LiuDepartment of Pathology, The Affiliated Hospital of Luzhou Medical College Zhongshan Road 319, Luzhou, 646000, China.
Jie ZhouDepartment of Neurosurgery, The Affiliated Hospital of Luzhou Medical College Taiping Road 25, Luzhou, 646000, China.
Cuiwei ZhangDepartment of Pathology, The Affiliated Hospital of Luzhou Medical College Zhongshan Road 319, Luzhou, 646000, China.
Wenguang FuDepartment of Hepatobiliary Surgery, The Affiliated Hospital of Luzhou Medical College Taiping Road 25, Luzhou, 646000, China.
Xiuli XiaoDepartment of Pathology, The Affiliated Hospital of Luzhou Medical College Zhongshan Road 319, Luzhou, 646000, China.
Sibei RuanDepartment of Pathology, The Affiliated Hospital of Luzhou Medical College Zhongshan Road 319, Luzhou, 646000, China.
Yuan ZhangDepartment of Pathology, The Affiliated Hospital of Luzhou Medical College Zhongshan Road 319, Luzhou, 646000, China.
Xia LuoDepartment of Pathology, The Affiliated Hospital of Luzhou Medical College Zhongshan Road 319, Luzhou, 646000, China.
Mingxi TangDepartment of Pathology, The Affiliated Hospital of Luzhou Medical College Zhongshan Road 319, Luzhou, 646000, China.
First Affiliated Hospital of Sichuan Medical University · CNAffiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The implication of HLJ1, a member of the heat shock protein-40 chaperone family, in colorectal carcinoma (CRC) remains unclear. The aim of this study was to determine the dynamic changes of HLJ1 in CRC both in vitro and in vivo, and the relationship between its level and the survival rate of CRC patients. Both real-time RT-PCR and Western blot were used to detect the expression of HLJ1 in CRC cells, while the distribution of HLJ1 in CRC and its adjacent normal mucosa tissues from CRC patients was determined with immunohistochemistry. Moreover, MTT and in vitro invasive assays were performed to determine the effect of HLJ1 overexpression on cell proliferation and invasion of CRC cells. The results indicated that in highly metastatic CRC cells, the HLJ1 expression was lower than that in lowly metastatic ones, and that the overexpression of HLJ1 significantly inhibited CRC cell proliferation and invasion in vitro. Interestingly, the HLJ1 expression was significantly down-regulated in CRC or lymphatic metastatic tissues from patient, compared to that in the normal mucosa (P<0.05), and the HLJ1 expression was correlated strongly with lymph metastasis, Dukes' stage, and remote metastasis (P<0.05). Most surprisingly, patients with a higher HLJ1 level had a better overall survival rate, compared to that in patients with lower HLJ1 level (P<0.05). Based on all these findings, we conclude that HLJ1 is a strong tumor suppressor for CRC, and thus the down-regulation of the HLJ1 expression may be used as a biomarker to predict clinical outcome of patients with CRC.

Indexed as

AdenocarcinomaBiomarkers, TumorBlotting, WesternColorectal NeoplasmsDisease ProgressionHSP40 Heat-Shock ProteinsHumansImmunohistochemistryKaplan-Meier EstimateProportional Hazards ModelsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionBiomarkers, TumorDNAJB4 protein, humanHSP40 Heat-Shock Proteinsbiomarkercolorectal carcinoma (CRC)HLJ1metastasissurvival rate

Identifiers

PMID24696714
PMCPMC3971299
OpenAlexW1445923311

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.