Evidence map›Paper›PMID 25271422›Full record

ArticlePloS one2014

BMP-2 promotes oral squamous carcinoma cell invasion by inducing CCL5 release.

Mi-joo Kim, Kwang-mahn Kim, Jin Kim, Kyoung-nam Kim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 27 citations in OpenAlex.

  1. Recombinant bone morphogenetic protein-2 attenuates colorectal cancer progression by orchestrating Hippo pathway activation, Yes-associated protein inhibition, and epithelial-mesenchymal transition suppression.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2026
    Article
  2. Cancers · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Transcriptomic characterization of differential gene expression in oral squamous cell carcinoma: a meta-analysis of publicly available microarray data sets.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  9. Article
  10. Review
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

4 authors at 2 institutions in 1 country.

Mi-joo KimDepartment and Research Institute of Dental Biomaterials and Bioengineering, Dental Devices Testing & Evaluation Center, Brain Korea 21 Plus project, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
Kwang-mahn KimDepartment and Research Institute of Dental Biomaterials and Bioengineering, Dental Devices Testing & Evaluation Center, Brain Korea 21 Plus project, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
Jin KimDepartment of Oral Pathology, Oral Cancer Research Institute, Brain Korea 21 Plus project, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
Kyoung-nam KimDepartment and Research Institute of Dental Biomaterials and Bioengineering, Dental Devices Testing & Evaluation Center, Brain Korea 21 Plus project, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
Yonsei University Dental Hospital · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone morphogenetic protein-2 (BMP-2)-containing bone grafts are useful regenerative materials for oral and maxillofacial surgery; however, several in vitro and in vivo studies previously reported cancer progression-related adverse effects caused by BMP-2. In this study, by quantifying the rhBMP-2 content released from bone grafts, the rhBMP-2 concentration that did not show cytotoxicity in each cell line was determined and applied to the in vitro monoculture or coculture model in the invasion assay. Our results showed that 1 ng/ml rhBMP-2, while not affecting cancer cell viability, significantly increased the invasion ability of the cancer cells cocultured with fibroblasts. Cocultured medium with rhBMP-2 also contained increased levels of matrix metalloproteinases. rhBMP-2-treated cocultured fibroblasts did not show a prominent difference in mRNA expression profile. Some cytokines, however, were detected in the conditioned medium by a human cytokine antibody array. Among them, the cancer invasion-related factor CCL5 was quantified by ELISA. Interestingly, CCL5 neutralizing antibodies significantly reduced the invasion of oral cancer cells. In conclusion, our results suggest that 1 ng/ml rhBMP-2 may induce invasion of oral squamous cell carcinoma (OSCC) cells by CCL5 release in coculture models. Therefore, we propose that a careful clinical examination before the use of rhBMP-2-containing biomaterials is indispensable for using rhBMP-2 treatment to prevent cancer progression.

Indexed as

Bone and BonesBone Morphogenetic Protein 2Carcinoma, Squamous CellCell Line, TumorCell SurvivalChemokine CCL5FibroblastsHumansMatrix MetalloproteinasesMouth NeoplasmsNeoplasm InvasivenessRecombinant ProteinsBone Morphogenetic Protein 2Chemokine CCL5Matrix MetalloproteinasesRecombinant Proteins

Identifiers

PMID25271422
PMCPMC4182698
OpenAlexW2088460216

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.