Evidence map›Paper›PMID 32637415›Full record

ArticleFrontiers in medicine2020

ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway.

Rui Zhou, William C S Cho, Victor Ma, Wah Cheuk, Yik-Ka So, S C Cesar Wong, Mingrong Zhang, Cong Li, Yujie Sun, Hong Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. A Theranostic Study ofBioconjugate chemistry · 2026
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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

12 authors at 6 institutions in 2 countries.

Rui ZhouDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
William C S ChoDepartment of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, China.
Victor MaDepartment of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, China.
Wah CheukDepartment of Pathology, Queen Elizabeth Hospital, Hong Kong, China.
Yik-Ka SoDepartment of Pathology, Queen Elizabeth Hospital, Hong Kong, China.
S C Cesar WongDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Mingrong ZhangDepartment of Advanced Nuclear Medicine Sciences, National Institute of Radiological Sciences, Chiba, Japan.
Cong LiKey Laboratory of Smart Drug Delivery, Ministry of Education, School of Pharmacy, Fudan University, Shanghai, China.
Yujie SunState Key Laboratory of Membrane Biology, Biomedical Pioneer Innovation Center, School of Life Sciences, Peking University, Beijing, China.
Hong ZhangDepartment of Nuclear Medicine and Medical PET Center, The Second Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Lawrence W C ChanDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Mei TianDepartment of Nuclear Medicine and Medical PET Center, The Second Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Queen Elizabeth Hospital · CNHong Kong Polytechnic University · HKSecond Affiliated Hospital of Zhejiang University · CNFudan University · CNPeking University · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Upregulation of a disintegrin and metalloprotease 9 (ADAM9) is correlated with progression of cancers, such as prostate, bladder, and pancreatic cancers. However, its role in triple-negative breast cancer (TNBC) is still unclear. Our study aimed to investigate whether ADAM9 is upregulated and promoted the aggressiveness in TNBC. Breast cancer cell lines and patient specimens were used to evaluate the ADAM9 expression by western blotting and immunohistochemistry staining, respectively. Compared with the non-TNBC, ADAM9 expression was significantly increased in TNBC cells and TNBC patient specimens. Based on the data acquired from public databases, the correlation between ADAM9 expression and breast cancer patient survival was analyzed by Kaplan-Meier method. It was shown that ADAM9 overexpression was significantly correlated with poorer survival in patients with TNBC. Furthermore, ADAM9 in TNBC cells was knocked down by small interference RNA and then studied by the MTT/colony formation assay, wound healing assay and transwell invasion assay on the cell proliferation, migration, and invasion, respectively. We found that inhibiting ADAM9 expression suppressed TNBC cell proliferation, migration, and invasion by lowering the activation of AKT/NF-κB pathway. Our results demonstrated that ADAM9 is an important molecule in mediating TNBC aggressiveness and may be a potential useful therapeutic target in TNBC treatment.

Indexed as

A disintegrin and metalloprotease 9 (ADAM9)AKTNF-κBtriple-negative breast cancer (TNBC)tumor progression

Identifiers

PMID32637415
PMCPMC7317048
OpenAlexW3033743293

What OpenQuestion holds

Textmetadata
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.