Evidence map›Paper›PMID 34439211›Full record

ArticleCancers2021

CD44 Promotes Lung Cancer Cell Metastasis through ERK-ZEB1 Signaling.

Yen-Yun Wang, Anupama Vadhan, Ping-Ho Chen, Yen-Lung Lee, Chih-Yeh Chao, Kuang-Hung Cheng, Yu-Chiuan Chang, Stephen Chu-Sung Hu, Shyng-Shiou F Yuan

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
5.1field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 60 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

9 authors at 3 institutions in 1 country.

Yen-Yun WangTranslational Research Center, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan.
Anupama VadhanGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Ping-Ho ChenSchool of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.ORCID 0000-0002-0357-8081
Yen-Lung LeeDepartment of Surgery, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan.
Chih-Yeh ChaoDepartment of Mechanical Engineering, National Pingtung University of Science and Technology, Pingtung 912, Taiwan.
Kuang-Hung ChengInstitute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan.
Yu-Chiuan ChangInstitute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan.
Stephen Chu-Sung HuDepartment of Dermatology, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Shyng-Shiou F YuanTranslational Research Center, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan.ORCID 0000-0002-4753-788X
Kaohsiung Medical University · TWNational Sun Yat-sen University · TWNational Pingtung University of Science and Technology · TW

Funding

Kaohsiung Medical University Hospital, Kaohsiung Medical University KMU-DK108005, Center for Cancer Research KMU-TC108A04-0, KMU-TC108A04-1, KMUH-DK(A)110001Ministry of Science and Technology, Taiwan MOHW110-TDU-B-212-144016
6 · The paper itself

Abstract

Lung cancer is a malignancy with high mortality worldwide, and metastasis occurs at a high frequency even when cancer spread is not detectable at primary operation. Cancer stemness plays an important role in malignant cancer behavior, treatment resistance, and cancer metastasis. Therefore, understanding the molecular pathogenesis behind cancer-stemness-mediated metastasis and developing effective approaches to prevent metastasis are key issues for improving cancer treatment. In this study, we investigated the role of CD44 stemness marker in lung cancer using in vitro and clinical studies. Immunohistochemical staining of lung cancer tissue specimens revealed that primary tumors with higher CD44 expression showed increased metastasis to regional lymph nodes. Flow cytometry analysis suggested that CD44 positive cells were enriched in the metastatic lymph nodes compared to the primary tumors. CD44 overexpression significantly increased migration and invasion abilities of lung cancer cells through CD44-induced ERK phosphorylation, ZEB1 upregulation, and Claudin-1 downregulation. Furthermore, ERK inhibition suppressed the migration and invasion abilities of CD44-overexpressing lung cancer cells. In summary, our in vitro and clinical results indicate that CD44 may be a potential prognostic and therapeutic marker for lung cancer patients.

Indexed as

CD44ERKlung cancermetastasisZEB1

Identifiers

PMID34439211
PMCPMC8392539
OpenAlexW3189451522

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.