Evidence map›Paper›PMID 31487123›Full record

ReviewCancer medicine2019

Taking a holistic view of PEST-containing nuclear protein (PCNP) in cancer biology.

Attia Afzal, Muhammad Sarfraz, Guang-Lei Li, Shao-Ping Ji, Shao-Feng Duan, Nazeer Hussain Khan, Dong-Dong Wu, Xin-Ying Ji

Open access · goldAbstract readReview
In one paragraph

Review in Cancer medicine, 2019. 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 33% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. The UHRF protein family in epigenetics, development, and carcinogenesis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    Review
  9. Article
  10. Review
  11. Observational
  12. Review
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

8 authors at 2 institutions in 2 countries.

Attia AfzalHenan International Joint Laboratory for Nuclear Protein Regulation, Henan University, Kaifeng, China.
Muhammad SarfrazHenan International Joint Laboratory for Nuclear Protein Regulation, Henan University, Kaifeng, China.
Guang-Lei LiHenan International Joint Laboratory for Nuclear Protein Regulation, Henan University, Kaifeng, China.
Shao-Ping JiMuncipal Key Laboratory of Cell Signal Transduction, Henan Provincial Engineering Centre for Tumor Molecular Medicine, Henan University, Kaifeng, China.
Shao-Feng DuanHenan International Joint Laboratory for Nuclear Protein Regulation, Henan University, Kaifeng, China.
Nazeer Hussain KhanHenan International Joint Laboratory for Nuclear Protein Regulation, Henan University, Kaifeng, China.
Dong-Dong WuHenan International Joint Laboratory for Nuclear Protein Regulation, Henan University, Kaifeng, China.
Xin-Ying JiHenan International Joint Laboratory for Nuclear Protein Regulation, Henan University, Kaifeng, China.ORCID 0000-0003-0690-4206
Henan University · CNUniversity of Lahore · PK

Funding

National Natural Science Foundation of China 81602708National Natural Science Foundation of China 81670088
6 · The paper itself

Abstract

Polypeptide sequences enriched with proline (P), glutamic acid (E), aspartic acid (D) and serine (S)/ threonine (T) (PEST) have been reported to be the most abundant and frequently distributed at the cellular level. There is growing evidence that PEST sequences act as proteolytic recognition signals for degradation of residual proteins which is critical for activation or deactivation of regulatory proteins involved in cellular signaling pathways of cell growth, differentiation, stress responses and physiological death. A PEST containing nuclear protein (PCNP) was demonstrated as a tumor suppressor in a neuroblastoma cancer model and tumor promoter in lung adenocarcinoma cancer model. Its unique properties like ubiquitination by NIRF, co-localization with NIRF in nucleus and tumor progression attract the attention of researchers. PCNP was reported to be ubiquitinated by ring finger protein NIRF in E3 ligase manner and as modulator of MAPK and PI3K/AKT/mTOR signaling pathways. In this review, we summarize PCNP linked DNA damage response, Post translational modifications, and transportation to address initiation, prognosis, and resistance of tumor cells in terms of cell cycle regulation, transcription and apoptosis. Hence, we demonstrate PCNP as a novel target in cancer diagnosis and treatment.

Indexed as

Adaptor Proteins, Signal TransducingAmino Acid SequenceCell CycleChromatinGene Expression Regulation, NeoplasticHumansNeoplasmsNuclear ProteinsProtein Processing, Post-TranslationalProtein TransportTranscription, GeneticUbiquitinationAdaptor Proteins, Signal TransducingChromatinNuclear ProteinsPCNP protein, humanapoptosisMAPKPCNPPESTSTATstumorUbiquitin

Identifiers

PMID31487123
PMCPMC6797571
OpenAlexW2972052177

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.