Evidence map›Paper›PMID 27437093›Full record

ArticleToxicological research2016

Tumorigenicity Evaluation of Umbilical Cord Blood-derived Mesenchymal Stem Cells.

Sang-Jin Park, Hyun-Jung Kim, Woojin Kim, Ok-Sun Kim, Sunyeong Lee, Su-Yeon Han, Eun Ju Jeong, Hyun-Shin Park, Hea-Won Kim, Kyoung-Sik Moon

Abstract read
In one paragraph

Article in Toxicological research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Review
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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

10 authors.

Sang-Jin ParkDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.
Hyun-Jung KimDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.
Woojin KimDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.
Ok-Sun KimDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.
Sunyeong LeeDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.
Su-Yeon HanDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.
Eun Ju JeongDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.
Hyun-Shin ParkResearch Institute, Genexine Co., Seongnam, Korea.
Hea-Won KimResearch Institute, Genexine Co., Seongnam, Korea.
Kyoung-Sik MoonDepartment of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have been identified in multiple types of tissue and exhibit characteristic self-renewal and multi-lineage differentiation abilities. However, the possibility of oncogenic transformation after transplantation is concerning. In this study, we investigated the tumorigenic potential of umbilical cord blood-derived MSCs (hUCB-MSCs) relative to MRC-5 and HeLa cells (negative and positive controls, respectively) both in vitro and in vivo. To evaluate tumorigenicity in vitro, anchorage-independent growth was assessed using the soft agar colony formation assay. hUCB-MSCs and MRC-5 cells formed few colonies, while HeLa cells formed a greater number of larger colonies, indicating that hUCB-MSCs and MRC-5 cells do not have anchorage-independent proliferation potential. To detect tumorigenicity in vivo, hUCB-MSCs were implanted as a single subcutaneous injection into BALB/c-nu mice. No tumor formation was observed in mice transplanted with hUCB-MSCs or MRC-5 cells based on macroand microscopic examinations; however, all mice transplanted with HeLa cells developed tumors that stained positive for a human gene according to immunohistochemical analysis. In conclusion, hUCB-MSCs do not exhibit tumorigenic potential based on in vitro and in vivo assays under our experimental conditions, providing further evidence of their safety for clinical applications.

Indexed as

ImmunohistochemistryMesenchymal stem cellsSoft agar assayTumorigenicity

Identifiers

PMID27437093
PMCPMC4946422

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Registered trials

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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.