Evidence map›Paper›PMID 27561949›Full record

ArticleExperimental & molecular medicine2016

Crucial role of HMGA1 in the self-renewal and drug resistance of ovarian cancer stem cells.

Dae Kyoung Kim, Eun Jin Seo, Eun J Choi, Su In Lee, Yang Woo Kwon, Il Ho Jang, Seung-Chul Kim, Ki-Hyung Kim, Dong-Soo Suh, Kim Seong-Jang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 58 citations in OpenAlex.

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  18. Therapeutic Strategies for Targeting Ovarian Cancer Stem Cells.International journal of molecular sciences · 2021
    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

12 authors at 2 institutions in 1 country.

Dae Kyoung KimDepartment of Physiology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Eun Jin SeoDepartment of Physiology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Eun J ChoiDepartment of Physiology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Su In LeeDepartment of Physiology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Yang Woo KwonDepartment of Physiology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Il Ho JangDepartment of Physiology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Seung-Chul KimDepartment of Obstetrics and Gynecology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Ki-Hyung KimDepartment of Obstetrics and Gynecology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Dong-Soo SuhDepartment of Obstetrics and Gynecology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Kim Seong-JangDepartment of Nuclear Medicine, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Sang Chul LeeFunctional Genomics Research Center, Korea Research Institute of Bioscience & Biotechnology, Daejeon, Republic of Korea.
Jae Ho KimDepartment of Physiology, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Pusan National University · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells are a subpopulation of cancer cells characterized by self-renewal ability, tumorigenesis and drug resistance. The aim of this study was to investigate the role of HMGA1, a chromatin remodeling factor abundantly expressed in many different cancers, in the regulation of cancer stem cells in ovarian cancer. Spheroid-forming cancer stem cells were isolated from A2780, SKOV3 and PA1 ovarian cancer cells by three-dimensional spheroid culture. Elevated expression of HMGA1 was observed in spheroid cells along with increased expression of stemness-related genes, such as SOX2, KLF4, ALDH, ABCB1 and ABCG2. Furthermore, spheroid A2780 cells, compared with adherent cells, showed higher resistance to chemotherapeutic agents such as paclitaxel and doxorubicin. HMGA1 knockdown in spheroid cells reduced the proliferative advantage and spheroid-forming efficiency of the cells and the expression of stemness-related genes. HMGA1 overexpression in adherent A2780 cells increased cancer stem cell properties, including proliferation, spheroid-forming efficiency and the expression of stemness-related genes. In addition, HMGA1 regulated ABCG2 promoter activity through HMGA1-binding sites. Knockdown of HMGA1 in spheroid cells reduced resistance to chemotherapeutic agents, whereas the overexpression of HMGA1 in adherent ovarian cancer cells increased resistance to chemotherapeutic agents in vitro. Furthermore, HMGA1-overexpressing A2780 cells showed a significant survival advantage after chemotherapeutic agent treatment in a xenograft tumorigenicity assay. Together, our results provide novel insights regarding the critical role of HMGA1 in the regulation of the cancer stem cell characteristics of ovarian cancer cells, thus suggesting that HMGA1 may be an important target in the development of therapeutics for ovarian cancer patients.

Indexed as

Cell ProliferationDrug Resistance, NeoplasmAnimalsAntineoplastic AgentsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHMGA1a ProteinHumansKruppel-Like Factor 4Mice, Inbred BALB CMice, NudeNeoplastic Stem CellsOvarian NeoplasmsOvarySpheroids, CellularAntineoplastic AgentsHMGA1a ProteinKLF4 protein, humanKlf4 protein, mouseKruppel-Like Factor 4

Identifiers

PMID27561949
PMCPMC5007643
OpenAlexW2511948892

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.