Evidence map›Paper›PMID 33760219›Full record

ArticleOncology reports2021

Bruton's agammaglobulinemia tyrosine kinase (Btk) regulates TPA‑induced breast cancer cell invasion via PLCγ2/PKCβ/NF‑κB/AP‑1‑dependent matrix metalloproteinase‑9 activation.

Jeong-Mi Kim, Jinny Park, Eun-Mi Noh, Hyun-Kyung Song, Sang Yull Kang, Sung Hoo Jung, Jong-Suk Kim, Byung-Hyun Park, Young-Rae Lee, Hyun Jo Youn

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Jeong-Mi Kim *Department of Biochemistry, Institute of Medical Science, Chonbuk National University Medical School, Jeonju, Jeollabuk 560‑182, Republic of Korea.
Jinny Park *Department of Internal Medicine, Division of Hematology, Gil Medical Center, Gachon University College of Medicine, Incheon 405‑760, Republic of Korea.
Eun-Mi NohDepartment of Oral Biochemistry, School of Dentistry, Wonkwang University, Iksan, Jeollabuk 570‑749, Republic of Korea.
Hyun-Kyung SongDepartment of Oral Biochemistry, School of Dentistry, Wonkwang University, Iksan, Jeollabuk 570‑749, Republic of Korea.
Sang Yull KangDepartment of Surgery, Research Institute of Clinical Medicine, Jeonbuk National University Hospital, Jeonbuk National University and Biomedical Research Institute, Jeonju, Jeollabuk 560‑182, Republic of Korea.
Sung Hoo JungDepartment of Surgery, Research Institute of Clinical Medicine, Jeonbuk National University Hospital, Jeonbuk National University and Biomedical Research Institute, Jeonju, Jeollabuk 560‑182, Republic of Korea.
Jong-Suk KimDepartment of Biochemistry, Institute of Medical Science, Chonbuk National University Medical School, Jeonju, Jeollabuk 560‑182, Republic of Korea.
Byung-Hyun ParkDepartment of Biochemistry and Molecular Biology and Director of Center for Meta Inflammation Research, Chonbuk National University Medical School, Jeonju, Jeonbuk 54896, Republic of Korea.
Young-Rae LeeDepartment of Oral Biochemistry, School of Dentistry, Wonkwang University, Iksan, Jeollabuk 570‑749, Republic of Korea.
Hyun Jo YounDepartment of Surgery, Research Institute of Clinical Medicine, Jeonbuk National University Hospital, Jeonbuk National University and Biomedical Research Institute, Jeonju, Jeollabuk 560‑182, Republic of Korea.
Jeonbuk National University · KRJeonbuk National University Hospital · KRWonkwang University · KRGachon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bruton's agammaglobulinemia tyrosine kinase (BTK) is an important cytoplasmic tyrosine kinase involved in B‑lymphocyte development, differentiation, and signaling. Activated protein kinase C (PKC), in turn, induces the activation of mitogen‑activated protein kinase (MAPK) signaling, which promotes cell proliferation, viability, apoptosis, and metastasis. This effect is associated with nuclear factor‑κB (NF‑κB) activation, suggesting an anti‑metastatic effect of BTK inhibitors on MCF‑7 cells that leads to the downregulation of matrix metalloproteinase (MMP)‑9 expression. However, the effect of BTK on breast cancer metastasis is unknown. In this study, the anti‑metastatic activity of BTK inhibitors was examined in MCF‑7 cells focusing on MMP‑9 expression in 12‑

Indexed as

AdenineAgammaglobulinaemia Tyrosine KinaseBreast NeoplasmsCell MovementFemaleGene Expression Regulation, NeoplasticHumansMAP Kinase Signaling SystemMatrix Metalloproteinase 9MCF-7 CellsNeoplasm InvasivenessNF-kappa BPhospholipase C gammaPiperidinesTetradecanoylphorbol AcetateTranscription Factor AP-1AdenineAgammaglobulinaemia Tyrosine KinaseBTK protein, humanibrutinibMatrix Metalloproteinase 9MMP9 protein, humanNF-kappa BPhospholipase C gammaPiperidinesPLCG2 protein, humanTetradecanoylphorbol AcetateTranscription Factor AP-1Bruton's agammaglobulinemia tyrosine kinasematrix metalloproteinase‑9MCF‑7 cellsprotein kinase C

Identifiers

PMID33760219
PMCPMC7962096
OpenAlexW3135842059

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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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.