Evidence map›Paper›PMID 26608371›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

CD24 promotes HCC progression via triggering Notch-related EMT and modulation of tumor microenvironment.

Xin Wan, Ci Cheng, Qing Shao, Zhe Lin, Shuai Lu, Yun Chen

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

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  5. Targeting CD24 as a novel immunotherapy for solid cancers.Cell communication and signaling : CCS · 2023
    Review
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  18. Dietary Phytochemicals Targeting Cancer Stem Cells.Molecules (Basel, Switzerland) · 2019
    Review
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  20. Article
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

6 authors at 2 institutions in 1 country.

Xin WanDepartment of Immunology, Nanjing Medical University, 140 Hanzhong Road, Nanjing, Jiangsu Province, People's Republic of China.
Ci ChengDepartment of Immunology, Nanjing Medical University, 140 Hanzhong Road, Nanjing, Jiangsu Province, People's Republic of China.
Qing ShaoDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu Province, People's Republic of China.
Zhe LinDepartment of Immunology, Nanjing Medical University, 140 Hanzhong Road, Nanjing, Jiangsu Province, People's Republic of China.
Shuai LuDepartment of Immunology, Nanjing Medical University, 140 Hanzhong Road, Nanjing, Jiangsu Province, People's Republic of China.
Yun ChenDepartment of Immunology, Nanjing Medical University, 140 Hanzhong Road, Nanjing, Jiangsu Province, People's Republic of China. chenyun@njmu.edu.cn.
Nanjing Medical University · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD24 is known as a cell surface molecule in hematopoiesis and also described as a diagnostic marker for tumors. Previous studies suggested the important role of CD24 in hepatocellular carcinoma (HCC) pathogenesis. However, precise functions of CD24 in HCC are still unknown. Here, we found that CD24 is highly expressed in HCC both in mRNA and protein levels. Further, the epithelial-mesenchymal transition (EMT) and Notch1 signaling activations mediated by CD24 were elucidated as potential mechanisms of HCC promotion in Hepa1-6/Hepa1-6-CD24 cell models. Additionally, possible systemic immune reaction was explored through immune cells and Hepa1-6/Hepa1-6-CD24 cell co-culture. We demonstrated that the EMT process of HCC cell was effectively induced by CD24; also, the tumor immune microenvironment was changed by facilitating Notch-related EMT in vivo. These results reveal the underlying link between the HCC processes mediated by CD24. Moreover, as a clear tumor promoter, CD24 is considered a potential new target for HCC treatment.

Indexed as

Epithelial-Mesenchymal TransitionTumor MicroenvironmentAnimalsCarcinoma, HepatocellularCD24 AntigenCell Line, TumorCell MovementCell Transformation, NeoplasticDendritic CellsDisease Models, AnimalDisease ProgressionHeterograftsHumansImmunomodulationLiver NeoplasmsMiceCD24 AntigenReceptors, NotchCD24Epithelial-mesenchymal transitionHepatocellular carcinomaNotch1Tumor immunity

Identifiers

PMID26608371
OpenAlexW2173939359

What OpenQuestion holds

Textmetadata
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.