Evidence map›Paper›PMID 14982852›Full record

ArticleThe American journal of pathology2004

ARK5 expression in colorectal cancer and its implications for tumor progression.

Gen-ichi Kusakai, Atsushi Suzuki, Tsutomu Ogura, Sin'ichi Miyamoto, Atsushi Ochiai, Michio Kaminishi, Hiroyasu Esumi

Abstract readComparative Study
In one paragraph

Article in The American journal of pathology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Development of the Pyrido[2,3-ACS medicinal chemistry letters · 2025
    Article
  5. Article
  6. Sensitivities and Dependencies ofMedicina (Kaunas, Lithuania) · 2022
    Article
  7. Article
  8. Article
  9. Role of ARK5 in cancer and other diseases (Review).Experimental and therapeutic medicine · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Expression level of NUAK1 in human nasopharyngeal carcinoma and its prognostic significance.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Salinomycin enhances doxorubicin sensitivity through reversing the epithelial-mesenchymal transition of cholangiocarcinoma cells by regulating ARK5.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2017
    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

7 authors.

Gen-ichi KusakaiInvestigative Treatment Division, National Cancer Center, Research Institute East, Kashiwa, Chiba, Japan.
Atsushi Suzuki
Tsutomu Ogura
Sin'ichi Miyamoto
Atsushi Ochiai
Michio Kaminishi
Hiroyasu Esumi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel member of the human AMPK family, ARK5, was recently discovered to be a key molecule in mediating cancer cell migration activity in human pancreas cancer cell line PANC-1, and its activation was found to be induced by Akt-dependent phosphorylation at Ser 600. DNA array analysis with 241 paired cDNAs from 13 different types of tumors and corresponding normal tissues derived from cancer patients revealed ARK5 overexpression in the samples of colorectal cancer. ARK5 expression was measured and an in vitro invasion assay was performed in six human colorectal cancer cell lines, WiDr, HCT-15, DLD-1, SW620, LoVo, and SW480, and since high invasion activity was concordant with higher ARK5 expression, ARK5 expression was examined in relation to tumor progression and metastatic activity in clinical samples. In 56 clinical samples of primary colorectal cancers and their liver metastases, higher ARK5 expression was observed in the samples from more advanced cases, and much higher expression was observed in the liver metastases. In situ hybridization analysis showed ARK5 overexpression in tumor cells. Based on these findings, we propose that ARK5 overexpression is involved in tumor progression of colon cancer clinically.

Indexed as

Biomarkers, TumorBlotting, NorthernBlotting, SouthernCell Line, TumorColorectal NeoplasmsDisease ProgressionHumansIn Situ HybridizationLiver NeoplasmsNeoplasm InvasivenessOligonucleotide Array Sequence AnalysisProtein KinasesRepressor ProteinsReverse Transcriptase Polymerase Chain ReactionTransfectionBiomarkers, TumorNUAK1 protein, humanProtein KinasesRepressor Proteins

Identifiers

PMID14982852
PMCPMC1614714

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.