Evidence map›Paper›PMID 32926529›Full record

ArticleThoracic cancer2020

HAX1 enhances the survival and metastasis of non-small cell lung cancer through the AKT/mTOR and MDM2/p53 signaling pathway.

Zhigang Liang, Yuan Zhong, Lifei Meng, Yi Chen, Yahui Liu, Aihua Wu, Xinjian Li, Mingsong Wang

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2020. 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
2.5field-weighted citation impact, top 10% 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, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Advances of E3 ligases in lung cancer.Biochemistry and biophysics reports · 2024
    Review
  4. Article
  5. Article
  6. Silencing of mAmerican journal of cancer research · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Advances in the study of CDC42 in the female reproductive system.Journal of cellular and molecular medicine · 2022
    Review
  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 4 institutions in 2 countries.

Zhigang LiangDepartment of Thoracic Surgery, Ningbo First Hospital, Ningbo, China.ORCID 0000-0002-2562-1781
Yuan ZhongDepartment of Cardiothoracic Surgery, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Lifei MengDepartment of Thoracic Surgery, Ningbo First Hospital, Ningbo, China.
Yi ChenDepartment of Thoracic Surgery, Ningbo First Hospital, Ningbo, China.
Yahui LiuDepartment of Thoracic Surgery, Ningbo First Hospital, Ningbo, China.
Aihua WuDepartment of Clinical Laboratory, Ningbo First Hospital, Ningbo, China.
Xinjian LiDepartment of Thoracic Surgery, Ningbo First Hospital, Ningbo, China.
Mingsong WangDepartment of Thoracic Surgery, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China.ORCID 0000-0003-3291-5849
Ningbo First Hospital · CNShanghai Jiao Tong University · CNXinHua Hospital · CNZero to Three · US

Funding

National Natural Science Foundation of China 81772459Natural Science Foundation of Ningbo 2016A610167Zhejiang Provincial Medicine and Health Technology Project 2017KY580
6 · The paper itself

Abstract

backgroundHS-1-associated protein-1 (HAX1) has been reported to be overexpressed in non-small cell lung cancer (NSCLC) tissues. However, the underlying mechanism of HAX1 in NSCLC has not previously been demonstrated. The present study investigated the role and underlying mechanism of HAX1 in NSCLC.

methodsThe HAX1 expression were confirmed in NSCLC tissues through TCGA database and qRT-PCR. Moreover, we performed qRT-PCR, Western blotting, Transwell assays, TUNEL assays and so on to evaluate the role of HAX1 in A549 and H1299 cell lines.

resultsmRNA expression of HAX1 was overexpressed in NSCLC tissues compared to adjacent normal tissues according to The Cancer Genome Atlas (TCGA) database. QRT-PCR assays showed that HAX1 mRNA expression was upregulated in NSCLC tissues. The high HAX1 mRNA levels were found to be positively associated with tumor size, TNM stage and lymphatic metastasis. Silencing of HAX1 promoted apoptosis and reduced invasion of A549 and H1299 cells by inhibiting the AKT/mTOR and MDM2/P53 signal pathway. AKT agonist SC79 could inhibit apoptosis and promote proliferation, migration and invasion of A549 and H1299 cells transfected with si-HAX1.

conclusionsThe present study provided a better understanding of HAX1 mechanism in NSCLC and potential therapeutic target for NSCLC.

Indexed as

Adaptor Proteins, Signal TransducingAdultAgedAged, 80 and overCarcinoma, Non-Small-Cell LungCell Line, TumorHumansLung NeoplasmsMiddle AgedProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-mdm2Signal TransductionTOR Serine-Threonine KinasesTransfectionTumor Suppressor Protein p53Young AdultAdaptor Proteins, Signal TransducingHAX1 protein, humanMDM2 protein, humanMTOR protein, humanProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-mdm2TOR Serine-Threonine KinasesTumor Suppressor Protein p53AKTHS-1-associated protein-1non-small cell lung cancer

Identifiers

PMID32926529
PMCPMC7606027
OpenAlexW3087653769

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.