Evidence map›Paper›PMID 30947381›Full record

ArticleFEBS open bio2019

PTPRK suppresses progression and chemo-resistance of colon cancer cells via direct inhibition of pro-oncogenic CD133.

Masashi Matsushita, Yusuke Mori, Kyosuke Uchiumi, Takehiro Ogata, Mizuyo Nakamura, Hiroyuki Yoda, Hiroaki Soda, Nobuhiro Takiguchi, Yoshihiro Nabeya, Osamu Shimozato and 1 more

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Masashi MatsushitaLaboratory of DNA Damage Signaling, Chiba Cancer Center Research Institute, Japan.
Yusuke MoriLaboratory of DNA Damage Signaling, Chiba Cancer Center Research Institute, Japan.
Kyosuke UchiumiLaboratory of DNA Damage Signaling, Chiba Cancer Center Research Institute, Japan.
Takehiro OgataLaboratory of DNA Damage Signaling, Chiba Cancer Center Research Institute, Japan.
Mizuyo NakamuraLaboratory of DNA Damage Signaling, Chiba Cancer Center Research Institute, Japan.
Hiroyuki YodaLaboratory of Cancer Genetics, Chiba Cancer Center Research Institute, Japan.ORCID 0000-0002-5528-8940
Hiroaki SodaDepartment of Esophago-Gastrointestinal Surgery, Chiba Cancer Center Hospital, Japan.
Nobuhiro TakiguchiDepartment of Esophago-Gastrointestinal Surgery, Chiba Cancer Center Hospital, Japan.
Yoshihiro NabeyaDepartment of Esophago-Gastrointestinal Surgery, Chiba Cancer Center Hospital, Japan.
Osamu ShimozatoLaboratory of DNA Damage Signaling, Chiba Cancer Center Research Institute, Japan.
Toshinori OzakiLaboratory of DNA Damage Signaling, Chiba Cancer Center Research Institute, Japan.
Chiba Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Receptor-type protein tyrosine phosphatase κ (PTPRK) is considered to be a candidate tumor suppressor. PTPRK dephosphorylates CD133, which is a stem cell marker; phosphorylated CD133 accelerates xenograft tumor growth of colon cancer cells through the activation of AKT, but the functional significance of this has remained elusive. In this study, we have demonstrated that knockdown of PTPRK potentiates the pro-oncogenic CD133-AKT pathway in colon cancer cells. Intriguingly, depletion of PTPRK significantly reduced sensitivity to the anti-cancer drug oxaliplatin and was accompanied by up-regulation of phosphorylation of Bad, a downstream target of AKT. Together, our present observations strongly suggest that the CD133-PTPRK axis plays a pivotal role in the regulation of colon cancer progression as well as drug resistance.

Indexed as

AC133 AntigenAntineoplastic AgentsCarcinogenesisCell Line, TumorCell ProliferationDisease ProgressionDrug ResistanceHEK293 CellsHT29 CellsHumansOxaliplatinPhosphorylationReceptor-Like Protein Tyrosine Phosphatases, Class 2Signal TransductionAC133 AntigenAntineoplastic AgentsOxaliplatinPROM1 protein, humanPTPRK protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 2CD133colon carcinomadrug resistanceprotein tyrosine phosphatasePTPRK

Identifiers

PMID30947381
PMCPMC6487712
OpenAlexW2933404358

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.