Evidence map›Paper›PMID 28042501›Full record

ArticleAmerican journal of cancer research2016

A new PDAC mouse model originated from iPSCs-converted pancreatic cancer stem cells (CSCcm).

Anna Sanchez Calle, Neha Nair, Aung KoKo Oo, Marta Prieto-Vila, Megumi Koga, Apriliana Cahya Khayrani, Maram Hussein, Laura Hurley, Arun Vaidyanath, Akimasa Seno and 4 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

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  18. Engineering of biomaterials for tumor modeling.Materials today. Advances · 2020
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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

14 authors at 1 institution in 1 country.

Anna Sanchez CalleDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Neha NairDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Aung KoKo OoDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Marta Prieto-VilaDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Megumi KogaDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Apriliana Cahya KhayraniDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Maram HusseinDepartment of Chemistry, Faculty of Science, Menoufia University Shebin El-Koam 32511, Egypt.
Laura HurleyCancer Biology Graduate Program, School of Medicine, Wayne State University 10 E Warren, Avenue, Suite 2215, Detroit, Michigan 48201, USA.
Arun VaidyanathDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Akimasa SenoDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Yoshiaki IwasakiDepartment of Gastroenterology and Hepatology, Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama 700-8558, Japan.
Malu CalleDepartment of Systems Biology, University of Vic Vic, Barcelona 08500, Spain.
Tomonari KasaiDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Masaharu SenoDepartment of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University 3.1.1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Okayama University · JP

Funding

TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
NCI NIH HHS T32 CA009531
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is the most representative form of pancreatic cancers. PDAC solid tumours are constituted of heterogeneous populations of cells including cancer stem cells (CSCs), differentiated cancer cells, desmoplastic stroma and immune cells. The identification and consequent isolation of pancreatic CSCs facilitated the generation of genetically engineered murine models. Nonetheless, the current models may not be representative for the spontaneous tumour occurrence. In the present study, we show the generation of a novel pancreatic iPSC-converted cancer stem cell lines (CSCcm) as a cutting-edge model for the study of PDAC. The CSCcm lines were achieved only by the influence of pancreatic cancer cell lines conditioned medium and were not subjected to any genetic manipulation. The xenografts tumours from CSCcm lines displayed histopathological features of ADM, PanIN and PDAC lesions. Further molecular characterization from RNA-sequencing analysis highlighted primary culture cell lines (1

Indexed as

Cancer stem cellsconditioned mediumCSCcmiPSCspancreatic cancerPDAC

Identifiers

PMID28042501
PMCPMC5199755
OpenAlexW2587496087

What OpenQuestion holds

Textmetadata
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.