Evidence map›Paper›PMID 24689055›Full record

ArticleBioMed research international2014

The low chamber pancreatic cancer cells had stem-like characteristics in modified transwell system: is it a novel method to identify and enrich cancer stem-like cells?

Dongqing Wang, Haitao Zhu, Yanfang Liu, Qing Liu, Xiaodong Xie, Yuepeng Zhou, Lirong Zhang, Yan Zhu, Zhijian Zhang, Zhaoliang Su

Abstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

  1. [The application and research progress ofZhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2018
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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.

Dongqing WangThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Haitao ZhuThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Yanfang LiuThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Qing LiuThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Xiaodong XieThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Yuepeng ZhouThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Lirong ZhangThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Yan ZhuThe Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.
Zhijian ZhangDepartment of Histology and Embryology, Center of Clinical Medicine and Laboratory, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu 212013, China.
Zhaoliang SuDepartment of Immunology, Center of Clinical Medicine and Laboratory, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu 212013, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells (CSCs) or cancer-initiating cells (CICs) play an important role in tumor initiation, progression, metastasis, chemoresistance, and recurrence. It is important to construct an effective method to identify and isolate CSCs for biotherapy of cancer. During the past years, many researchers had paid more attention to it; however, this method was still on seeking. Therefore, compared to the former methods that were used to isolate the cancer stem cell, in the present study, we tried to use modified transwell system to isolate and enrich CSCs from human pancreatic cancer cell lines (Panc-1). Our results clearly showed that the lower chamber cells in modified transwell system were easily forming spheres; furthermore, these spheres expressed high levels of stem cell markers (CD133/CD44/CD24/Oct-4/ESA) and exhibited chemoresistance, underwent epithelial-to-mesenchymal transition (EMT), and possessed the properties of self-renewal in vitro and tumorigenicity in vivo. Therefore, we speculated that modified transwell assay system, as a rapid and effective method, can be used to isolate and enrich CSCs.

Indexed as

AC133 AntigenAnimalsAntigens, CDBiomarkers, TumorCarcinogenesisCell CountCell Culture TechniquesCell Line, TumorCell ProliferationCell SurvivalDeoxycytidineDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionGemcitabineGlycoproteinsHumansAC133 AntigenAntigens, CDBiomarkers, TumorDeoxycytidineGemcitabineGlycoproteinsHyaluronan ReceptorsPeptidesPROM1 protein, humanProm1 protein, mouse

Identifiers

PMID24689055
PMCPMC3934619

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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.