Evidence map›Paper›PMID 31905966›Full record

ArticleCancers2019

Impact of FAK Expression on the Cytotoxic Effects of CIK Therapy in Triple-Negative Breast Cancer.

Mei-Ren Pan, Cheng-Che Wu, Jung-Yu Kan, Qiao-Lin Li, Shu-Jyuan Chang, Chun-Chieh Wu, Chung-Liang Li, Fu Ou-Yang, Ming-Feng Hou, Hon-Kan Yip and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancers, 2019. 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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Mei-Ren PanGraduate Institute of Clinical Medicine, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.ORCID 0000-0003-2039-7570
Cheng-Che WuDepartment of Surgery, Kaohsiung Medical University Hospital, Kaohsiung 80756, Taiwan.
Jung-Yu KanDepartment of Surgery, Kaohsiung Medical University Hospital, Kaohsiung 80756, Taiwan.
Qiao-Lin LiGraduate Institute of Clinical Medicine, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.
Shu-Jyuan ChangGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.ORCID 0000-0002-1355-6820
Chun-Chieh WuDrug Development and Value Creation Research Center, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.
Chung-Liang LiDepartment of Surgery, Kaohsiung Medical University Hospital, Kaohsiung 80756, Taiwan.
Fu Ou-YangDrug Development and Value Creation Research Center, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.
Ming-Feng HouGraduate Institute of Clinical Medicine, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.
Hon-Kan YipDivision of Cardiology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan.
Chi-Wen LuoDrug Development and Value Creation Research Center, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.
Kaohsiung Medical University · TWKaohsiung Chang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is a special subtype of breast cancer in which several common diagnostic biomarkers are lost. Due to the loss of expression of receptors, treatment options for TNBC are limited. Therefore, finding safe and effective treatments for patients with TNBC is a major objective for clinicians. Previous studies suggested that cytokine-induced killer (CIK) cells may be beneficial for patients with a variety of tumor types. However, CIK therapy is not effective for all patients. In this study, we found that focal adhesion kinase (FAK), a non-receptor protein tyrosine kinase that regulates several cellular functions in different cells, has the potential to regulate tumor cells sensitized to CIK cells. Knockdown of FAK expression in TNBC cells or the treatment of TNBC cells with a FAK inhibitor followed by coculture with CIK cells increases death of TNBC cells, suggesting that FAK plays important roles in sensitizing tumor cells to CIK cells. This phenomenon could be regulated by a FAK-programmed death-ligand 1 (PD-L1)-related mechanism. Overall, our findings provide new insights into the cytotoxic effect of CIK cell therapy in TNBC treatment, and show that CIK cell therapy combined with FAK inhibitors may be a novel therapeutic strategy for patients with TNBC.

Indexed as

apoptosiscytokine induced killer cells (CIK)cytotoxicityfocal adhesion kinase (FAK)programmed death-ligand 1 (PD-L1)triple-negative breast cancer (TNBC)

Identifiers

PMID31905966
PMCPMC7017032
OpenAlexW2997040555

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.