Evidence map›Paper›PMID 26824320›Full record

ArticleOncotarget2016

Lapatinib inhibits CIP2A/PP2A/p-Akt signaling and induces apoptosis in triple negative breast cancer cells.

Chun-Yu Liu, Ming-Hung Hu, Chia-Jung Hsu, Chun-Teng Huang, Duen-Shian Wang, Wen-Chun Tsai, Yi-Ting Chen, Chia-Han Lee, Pei-Yi Chu, Chia-Chi Hsu and 4 more

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

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  12. [Screening of drugs that selectively inhibit uveal melanoma cells with SF3B1 mutations].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 1 country.

Chun-Yu LiuDivision of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Ming-Hung HuDivision of Hematology and Oncology, Department of Medicine, Cardinal Tien Hospital, New Taipei City, Taiwan.
Chia-Jung HsuDivision of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Chun-Teng HuangSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Duen-Shian WangDivision of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Wen-Chun TsaiDivision of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Yi-Ting ChenDivision of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Chia-Han LeeDivision of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Pei-Yi ChuDepartment of Pathology, Show Chwan Memorial Hospital, Changhua City, Taiwan.
Chia-Chi HsuInstitute of Pharmacology, National Yang-Ming University, Taipei, Taiwan.
Ming-Huang ChenDivision of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Chung-Wai ShiauInstitute of Biopharmaceutical Sciences, National Yang-Ming University, Taipei, Taiwan.
Ling-Ming TsengSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Kuen-Feng ChenDepartment of Medical Research, National Taiwan University Hospital, Taipei, Taiwan.
Taipei Veterans General Hospital · TWNational Yang Ming Chiao Tung University · TWChang Bing Show Chwan Memorial Hospital · TWFu Jen Catholic University · TWNational Yang Ming Chiao Tung University · TWTaipei City Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We tested the efficacy of lapatinib, a dual tyrosine kinase inhibitor which interrupts the HER2 and epidermal growth factor receptor (EGFR) pathways, in a panel of triple-negative breast cancer (TNBC) cells, and examined the drug mechanism. Lapatinib showed an anti-proliferative effect in HCC 1937, MDA-MB-468, and MDA-MB-231 cell lines. Lapatinib induced significant apoptosis and inhibited CIP2A and p-Akt in a dose and time-dependent manner in the three TNBC cell lines. Overexpression of CIP2A reduced lapatinib-induced apoptosis in MDA-MB-468 cells. In addition, lapatinib increased PP2A activity (in relation to CIP2A inhibition). Moreover, lapatinib-induced apoptosis and p-Akt downregulation was attenuated by PP2A antagonist okadaic acid. Furthermore, lapatinib indirectly decreased CIP2A transcription by disturbing the binding of Elk1 to the CIP2A promoter. Importantly, lapatinib showed anti-tumor activity in mice bearing MDA-MB-468 xenograft tumors, and suppressed CIP2A as well as p-Akt in these xenografted tumors. In summary, inhibition of CIP2A determines the effects of lapatinib-induced apoptosis in TNBC cells. In addition to being a dual tyrosine kinase inhibitor of HER2 and EGFR, lapatinib also inhibits CIP2A/PP2A/p-Akt signaling in TNBC cells.

Indexed as

AnimalsAntineoplastic AgentsApoptosisAutoantigensCell Line, TumorDisease Models, AnimalErb-b2 Receptor Tyrosine KinasesErbB ReceptorsHumansLapatinibMCF-7 CellsMembrane ProteinsMiceMice, NudePromoter Regions, GeneticProtein Kinase InhibitorsAntineoplastic AgentsAutoantigensEGFR protein, mouseErbb2 protein, mouseErb-b2 Receptor Tyrosine KinasesErbB ReceptorsKIAA1524 protein, mouseLapatinibMembrane ProteinsProtein Kinase InhibitorsProtein Phosphatase 2Proto-Oncogene Proteins c-aktQuinazolinesapoptosisCIP2AlapatinibPP2Atriple-negative breast cancer

Identifiers

PMID26824320
PMCPMC4891031
OpenAlexW2275209600

What OpenQuestion holds

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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.