Evidence map›Paper›PMID 30410860›Full record

ArticleFEBS open bio2018

Both Ser361 phosphorylation and the C-arrestin domain of thioredoxin interacting protein are important for cell cycle blockade at the G1/S checkpoint.

Kazuyo Kamitori, Fuminori Yamaguchi, Youyi Dong, Akram Hossain, Ayako Katagi, Chisato Noguchi, Yuko Hirata, Ikuko Tsukamoto, Naoya Hatano, Masaaki Tokuda

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Jab1/Cops5: a promising target for cancer diagnosis and therapy.International journal of clinical oncology · 2021
    Review
  10. Article
  11. Review
  12. 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

10 authors at 2 institutions in 1 country.

Kazuyo KamitoriDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Fuminori YamaguchiDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Youyi DongDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Akram HossainDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Ayako KatagiDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Chisato NoguchiDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Yuko HirataDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Ikuko TsukamotoDepartment of Pharmaco-Bio-Informatics Faculty of Medicine Kagawa University Miki-cho Japan.
Naoya HatanoIntegrated Center for Mass Spectrometry Kobe University Graduate School of Medicine Japan.
Masaaki TokudaDepartments of Cell Physiology Faculty of Medicine Kagawa University Miki-cho Japan.
Kagawa University · JPKobe University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thioredoxin interacting protein (TXNIP) is a novel tumor suppressor that is down-regulated in several cancer tissues and tumor cell lines. Overexpression of TXNIP causes cell cycle arrest at the G1/S checkpoint in the hepatocellular carcinoma cell line HuH-7. TXNIP contains putative phosphorylation sites, but the effects of its phosphorylation have not been fully characterized. TXNIP also contains two α-arrestin domains (N-arrestin and C-arrestin) whose functions are not fully understood. Here, we reveal an association between TXNIP and cell cycle regulatory proteins (p27

Indexed as

anti‐tumorarrestincell cyclep27kip1p38 MAPKTXNIP

Identifiers

PMID30410860
PMCPMC6212649
OpenAlexW2891688761

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.