Evidence map›Paper›PMID 39466654›Full record

ArticleJournal of cellular and molecular medicine2024

Bone sialoprotein facilitates anoikis resistance in lung cancer by inhibiting miR-150-5p expression.

Le Huynh Hoai Thuong, Chang-Lun Huang, Yi-Chin Fong, Chun-Lin Liu, Jeng-Hung Guo, Chih-Ying Wu, Po-I Liu, Chih-Hsin Tang

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

8 authors.

Le Huynh Hoai ThuongGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Chang-Lun HuangDivision of General Thoracic Surgery, Department of Surgery, Changhua Christian Hospital, Changhua, Taiwan.
Yi-Chin FongDepartment of Sports Medicine, College of Health Care, China Medical University, Taichung, Taiwan.
Chun-Lin LiuGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Jeng-Hung GuoGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Chih-Ying WuDepartment of Neurosurgery, China Medical University Hospital, Taichung, Taiwan.
Po-I LiuDepartment of Physical Therapy, Asia University, Taichung, Taiwan.
Chih-Hsin TangGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.ORCID 0000-0002-7113-8352

Funding

Asia University Hospital 11051008;11151019China Medical University CMU113-ASIA-001; CMU113-ASIA-05China Medical University Hospital DMR-112-081; DMR-111-095; DMR-112-146; DMR-112-218China Medical University under the Higher Education Sprout Project, Ministry of Education, Taiwan CMRC-CENTER-7Taiwan's Ministry of Science and Technology MOST 111-2314-B-039-048-MY3; NSTC 113-2320-B-371-0
6 · The paper itself

Abstract

Metastatic lung cancer is a highly prevalent cancer with a very low chance of long-term survival. Metastasis at secondary sites requires that cancer cells develop anoikis resistance to survive during circulation. High levels of bone sialoprotein (BSP), a member of the small integrin-binding ligand N-linked glycoproteins (SIBLINGs), have been shown to promote the spread of lung cancer cells; however, the effects of BSP in anoikis resistance are largely unknown. In this study, we determined that BSP promotes anoikis resistance in lung cancer cells. BSP was also shown to promote the expression of E-cadherin and vimentin (epithelial-to-mesenchymal transition markers, which have been utilized as indicators of anoikis resistance). It appears that BSP facilitates MMP-14-dependent anoikis resistance by inhibiting the synthesis of miR-150-5p and activating the ERK signalling pathway. Knockdown of BSP expression was shown to block lung cancer metastasis by lowering anoikis resistance in vivo. These results indicate that BSP is a promising target to deal with anoikis resistance and metastasis in human lung cancers.

Indexed as

AnoikisGene Expression Regulation, NeoplasticIntegrin-Binding SialoproteinLung NeoplasmsMicroRNAsA549 CellsAnimalsCadherinsCell Line, TumorEpithelial-Mesenchymal TransitionHumansMAP Kinase Signaling SystemMiceMice, NudeVimentinCadherinsIntegrin-Binding SialoproteinMicroRNAsMIR150, humanVimentinanoikis resistanceBSPlung cancermiR‐150‐5p

Identifiers

PMID39466654
PMCPMC11514928

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.