Evidence map›Paper›PMID 30783426›Full record

ArticleExperimental and therapeutic medicine2019

3D culture enhances chemoresistance of ALL Jurkat cell line by increasing DDR1 expression.

Jun Guo, Chunting Zhao, Ruyong Yao, Aihua Sui, Lingjie Sun, Xiaodan Liu, Shaoling Wu, Zhan Su, Tianlan Li, Shanshan Liu and 8 more

Abstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  9. Article
  10. Complex roles of discoidin domain receptor tyrosine kinases in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Review
  11. Article
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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

18 authors.

Jun GuoCollege of Medicine, Qingdao University, Qingdao, Shandong 266071, P.R. China.
Chunting ZhaoDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Ruyong YaoCentral Laboratory, Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong 266035, P.R. China.
Aihua SuiCentral Laboratory, Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong 266035, P.R. China.
Lingjie SunDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Xiaodan LiuDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Shaoling WuDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Zhan SuDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Tianlan LiDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Shanshan LiuDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Yan GaoDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Jiaxiu LiuCentral Laboratory, Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong 266035, P.R. China.
Xianqi FengDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Wei WangDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Hongguo ZhaoDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Zhongguang CuiDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Guanglun LiDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.
Fanjun MengDepartment of Hematology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266555, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three dimensional (3D) culture has gradually become a research hotspot in the field of drug screening, stem cell research, and tissue engineering due to its more physiological-like morphology and function. In this study, we compared the differences of cell proliferation, population, protein expression and chemoresistance profiles between two dimensional (2D) and 3D culture of acute lymphoblastic leukemia (ALL) Jurkat cell line. Polycaprolactone (PCL) is used for 3D culture owing to its biochemical properties and compatibility. Culturing of ALL Jurkat cell line in collagen type I coated polycaprolactone scaffold for 168 h increased cell proliferation, attachment, as well as the drug resistance to cytarabine (Ara-C) and daunorubicin (DNR) without changing the original CD2

Indexed as

3D culturecytarabinedaunorubicindiscoidin domain receptor 1resistance

Identifiers

PMID30783426
PMCPMC6364197

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.