Evidence map›Paper›PMID 20587145›Full record

ArticleCell transplantation2010

Isolation and propagation of a human CD133(-) colon tumor-derived cell line with tumorigenic and angiogenic properties.

Nalú Navarro-Alvarez, Eisaku Kondo, Hironobu Kawamoto, Wael Hassan, Takeshi Yuasa, Yasuhiro Kubota, Masayuki Seita, Hiroyuki Nakahara, Takahiro Hayashi, Yuriko Nishikawa and 8 more

Open access · greenAbstract read
In one paragraph

Article in Cell transplantation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Cancer stem cells in human digestive tract malignancies.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Rapid re-expression of CD133 protein in colorectal cancer cell lines in vitro and in vivo.Laboratory investigation; a journal of technical methods and pathology · 2012
    Article
  14. Lessons from common markers of tumor-initiating cells in solid cancers.Cellular and molecular life sciences : CMLS · 2011
    Review
  15. Article
  16. Article
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 at 3 institutions in 2 countries.

Nalú Navarro-AlvarezDepartment of Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Eisaku Kondo
Hironobu Kawamoto
Wael Hassan
Takeshi Yuasa
Yasuhiro Kubota
Masayuki Seita
Hiroyuki Nakahara
Takahiro Hayashi
Yuriko Nishikawa
Reham A R A Hassan
Shahid M Javed
Hirofumi Noguchi
Shinichi Matsumoto
Shuhei Nakaji
Noriaki Tanaka
Naoya Kobayashi
Alejandro Soto-Gutierrez
Okayama University · JPChildren's Hospital of Pittsburgh · USOkayama University of Science · JP

Funding

Engineering of hepatic grafts with decellularized native matricesK99DK083556 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SOTO-GUTIERREZ, ALEJANDRO · 2009 to 2010
$180k
NIDDK NIH HHS K99 DK083556
6 · The paper itself

Abstract

It has been proposed in human colorectal cancers (CRC) a minority subset of cancer cells within tumors able to initiate tumor growth, defined as cancer stem cells (CSC). Solid human primary colonic and its ovarian metastatic cancer tissues were collected from fresh surgical samples and subsequent xenografts were established in nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. The resulting tumors were disaggregated into single-cell suspensions and a CD133(-) cell line (NANK) was newly established and analyzed by flow cytometry. Surface markers of progenitor cells were immunophenotypically analyzed, and expression of stem cell and cancer-related genes was characterized. Secreted angiogenesis-associated molecules were investigated by proteomic array technology. Finally, different numbers of NANK were implanted and their tumor-initiating properties were investigated in NOD/SCID mice. Intraperitoneal injection of NANK in NOD/SCID mice induced tumors with developing progressive peritoneal dissemination and ascites. NANK cells maintained a differentiated phenotype and reproduced the full morphologic and phenotypic heterogeneity of their parental lesions. Noticeably, NANK lacked the expression of conventional CSC markers CD133 and CD44, self-renewal genes Oct-4 and Nanog, but showed the expression of an important gastrointestinal development marker CDX-2 and BMI-1 that is essential in regulating the proliferative activity of normal and leukemic stem cells. In addition, NANK secreted high amounts of important angiogenic cytokines. These results provide a novel and extensive model in human CSC for studying the generation and maintenance of phenotypic heterogeneity in CRC.

Indexed as

AC133 AntigenAdultAnimalsAntigens, CDBiomarkers, TumorCell Line, TumorCell ProliferationCell SeparationColonic NeoplasmsCytokinesFemaleGlycoproteinsHumansIntercellular Signaling Peptides and ProteinsMiceNeoplastic Stem CellsAC133 AntigenAntigens, CDBiomarkers, TumorCytokinesGlycoproteinsIntercellular Signaling Peptides and ProteinsPeptidesPROM1 protein, humanProm1 protein, mouse

Identifiers

PMID20587145
PMCPMC2957535
OpenAlexW2080148300

What OpenQuestion holds

Textmetadata
LicenceTDM
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.