Evidence map›Paper›PMID 29477378›Full record

ArticleCancer letters2018

ICAM3 mediates inflammatory signaling to promote cancer cell stemness.

Wenzhi Shen, Junling Xie, Shuangtao Zhao, Renle Du, Xiaohe Luo, Huiwen He, Shan Jiang, Na Hao, Chong Chen, Chunlei Guo and 7 more

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.5field-weighted citation impact, top 14% 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, 40 citations in OpenAlex.

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  16. ABI2-mediated MEOX2/KLF4-NANOG axis promotes liver cancer stem cell and drives tumour recurrence.Liver international : official journal of the International Association for the Study of the Liver · 2022
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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

17 authors at 6 institutions in 2 countries.

Wenzhi ShenDept. of Immunology, Institute of Basic Medical Science, Chinese Academy of Medical Science, School of Basic Medicine Peking Union Medical College, Beijing, 100005, China; Dept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China; International Joint Center for Biomedical Research of the Ministry of Education, Tianjin 300071, China; Dept. of Pathology and Institute of Precision Medicine, Jining Medical University, Jining 272067, China.
Junling XieDept. of Immunology, Institute of Basic Medical Science, Chinese Academy of Medical Science, School of Basic Medicine Peking Union Medical College, Beijing, 100005, China; Dept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center for Biotherapy, School of Basic Medical Science, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, 100005, China.
Shuangtao ZhaoDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China.
Renle DuDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China.
Xiaohe LuoDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China.
Huiwen HeDept. of Immunology, Institute of Basic Medical Science, Chinese Academy of Medical Science, School of Basic Medicine Peking Union Medical College, Beijing, 100005, China; Collaborative Innovation Center for Biotherapy, School of Basic Medical Science, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, 100005, China.
Shan JiangDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China.
Na HaoDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China.
Chong ChenDept. of Immunology, Institute of Basic Medical Science, Chinese Academy of Medical Science, School of Basic Medicine Peking Union Medical College, Beijing, 100005, China; Collaborative Innovation Center for Biotherapy, School of Basic Medical Science, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, 100005, China.
Chunlei GuoDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China.
Yanhua LiuDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China; International Joint Center for Biomedical Research of the Ministry of Education, Tianjin 300071, China.
Yanan ChenDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China; International Joint Center for Biomedical Research of the Ministry of Education, Tianjin 300071, China.
Peiqing SunDept. of Cancer Biology and Comprehensive Cancer Center, Wake Forest University Medical Center, Medical Blvd, Winston-Salem, NC 27157, USA.
Shengyong YangWest China Hospital, Molecular Medicine Research Centre, State Key Lab Biotherapy, Sichuan University, Chengdu 610064, China.
Na LuoDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China.
Rong XiangDept. of Immunology, School of Medicine, Nankai University, Tianjin, 300071, China; International Joint Center for Biomedical Research of the Ministry of Education, Tianjin 300071, China.
Yunping LuoDept. of Immunology, Institute of Basic Medical Science, Chinese Academy of Medical Science, School of Basic Medicine Peking Union Medical College, Beijing, 100005, China; Collaborative Innovation Center for Biotherapy, School of Basic Medical Science, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, 100005, China. Electronic address: ypluo@ibms.pumc.edu.cn.
Nankai University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNTianjin International Joint Academy of Biomedicine · CNJining Medical University · CNSichuan University · CNWake Forest University · US

Funding

Tip60 in p38 and PRAK Mediated Oncogene-Induced Senescence and Tumor SuppressionR01CA131231 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUN, PEIQING · 2009 to 2018
$3.5M
The role of microRNA in oncogene-induced senescence and cancer developmentR01CA172115 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUN, PEIQING · 2014 to 2018
$1.8M
NCI NIH HHS R01 CA131231NCI NIH HHS R01 CA172115
6 · The paper itself

Abstract

In this study, we present a medium throughput siRNA screen platform to identify inflammation genes that regulate cancer cell stemness. We identified several novel candidates that decrease OCT4 expression and reduce the ALDH + subpopulation both of which are characteristic of stemness. Furthermore, one of the novel candidates ICAM3 up-regulates in the ALDH + subpopulation, the side population and the developed spheres. ICAM3 knockdown reduces the side population, sphere formation and chemo-resistance in MDA-MB-231 human breast cancer cells and A549 lung cancer cells. In addition, mice bearing MDA-MB-231-shICAM3 cells develop smaller tumors and fewer lung metastases versus control. Interestingly, ICAM3 recruits and binds to Src by the YLPL motif in its intracellular domain which further activates the PI3K-AKT phosphorylation cascades. The activated p-AKT enhances SOX2 and OCT4 activity and thereby maintains cancer cell stemness. Meanwhile, the p-AKT facilitated p50 nuclear translocation/activation enhances p50 feedback and thereby promotes ICAM3 expression by binding to the ICAM3 promoter region. On this basis, Src and PI3K inhibitors suppress ICAM3-mediated signaling pathways and reduce chemo-resistance which results in tumor growth suppression in vitro and in vivo. In summary, we identify a potential CSC regulator and suggest a novel mechanism by which ICAM3 governs cancer cell stemness and inflammation.

Indexed as

Signal TransductionAnimalsAntigens, CDBiomarkersCell Adhesion MoleculesCell Line, TumorComputational BiologyDrug Resistance, NeoplasmGene Expression ProfilingGene Expression Regulation, NeoplasticHumansInflammationMiceNeoplasmsNeoplastic Stem CellsRNA, Small InterferingAntigens, CDBiomarkersCell Adhesion MoleculesICAM3 protein, humanRNA, Small InterferingCancer cell stemnessChemo-resistanceICAM3InflammationSiRNA screen

Identifiers

PMID29477378
PMCPMC5928798
OpenAlexW2792892721

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.