Evidence map›Paper›PMID 26339377›Full record

ArticleInternational journal of clinical and experimental pathology2015

HAX-1 is overexpressed in hepatocellular carcinoma and promotes cell proliferation.

Yanxia Wang, Xin Huo, Zheng Cao, Hui Xu, Jian Zhu, Li Qian, Hong Fu, Bing Xu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. High expression of HAX-1 protein is associated with tumor growth in papillary thyroid carcinoma.International journal of clinical and experimental pathology · 2018
    Article
  12. Article
  13. 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

8 authors at 1 institution in 1 country.

Yanxia WangDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Xin HuoDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Zheng CaoDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Hui XuDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Jian ZhuDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Li QianDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Hong FuDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Bing XuDepartment of Emergency, Shanghai Ninth People's Hospital Affiliated to Medicine College, Shanghai Jiao Tong University Shanghai 200011, China.
Shanghai Ninth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common primary liver tumor. Due to the asymptomatic nature of early HCC and lack of effective screening strategies, 80% of patients present with advanced HCC at the time of diagnosis. Novel molecular marker identification will be valuable for effective diagnosis and treatment. In this study we reported HCLS1-associated protein X-1 (HAX-1) is overexpression in HCC in human HCC sample. Furthermore, we provided evidence that HAX-1 expression positively correlated with that of Ki67 in patient sample. Statistic analysis indicated that HAX-1 expression level significantly correlated with clinic outcome of HCC. Cell based assay revealed that knockdown of HAX-1 inhibits cell proliferation. This result suggests that HAX-1 can be a novel molecular marker for HCC.

Indexed as

Cell ProliferationAdaptor Proteins, Signal TransducingAdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, HepatocellularCell Line, TumorFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansKaplan-Meier EstimateLiver NeoplasmsMaleMiddle AgedAdaptor Proteins, Signal TransducingBiomarkers, TumorHAX1 protein, humancell proliferationHAX-1Human hepatocellular carcinoma (HCC)

Identifiers

PMID26339377
PMCPMC4555705
OpenAlexW2460305717

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.