Evidence map›Paper›PMID 27694835›Full record

ArticleOncogenesis2016

The interplay between HPIP and casein kinase 1α promotes renal cell carcinoma growth and metastasis via activation of mTOR pathway.

H Mai, X Xu, G Mei, T Hong, J Huang, T Wang, Z Yan, Y Li, Y Liang, L Li and 5 more

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2016. 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
1.9field-weighted citation impact, top 14% 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, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Casein kinase 1α mediates eryptosis: a review.Apoptosis : an international journal on programmed cell death · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Casein kinase 1α: biological mechanisms and theranostic potential.Cell communication and signaling : CCS · 2018
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  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

15 authors at 2 institutions in 1 country.

H MaiDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
X XuDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
G MeiDepartment of Urology, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, People's Republic of China.
T HongDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
J HuangDepartment of Urology, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, People's Republic of China.
T WangDepartment of Oncology, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, People's Republic of China.
Z YanDepartment of Gynecology and Obstetrics, PLA General Hospital, Beijing, People's Republic of China.
Y LiDepartment of Oncology, PLA General Hospital, Beijing, People's Republic of China.
Y LiangDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
L LiDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
S JinDepartment of Thoracic Surgery, PLA General Hospital, Beijing, People's Republic of China.
W YouDepartment of Oncology, PLA General Hospital, Beijing, People's Republic of China.
Y MaDepartment of Thoracic Surgery, PLA General Hospital, Beijing, People's Republic of China.
L ChenDepartment of Urology, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, People's Republic of China.
Q YeDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Chinese PLA General Hospital · CNAcademy of Military Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic pre-B cell leukemia transcription factor (PBX)-interacting protein (HPIP) was shown to be crucial during the development and progression of a variety of tumors. However, the role of HPIP in renal cell carcinoma (RCC) is unknown. Here we report that HPIP is upregulated in most RCC patients, positively correlates with tumor size, high Fuhrman grade and preoperative metastasis, and predicts poor clinical outcomes. Mechanistically, we identified casein kinase 1α (CK1α), a critical regulator of tumorigenesis and metastasis, as a novel HPIP-interacting protein. HPIP facilitates RCC cell growth, migration, invasion and epithelial-mesenchymal transition depending on its interaction with CK1α. Activation of mammalian target of rapamycin pathways by HPIP is partly dependent on CK1α and is required for HPIP modulation of RCC cell proliferation and migration. HPIP knockdown suppresses renal tumor growth and metastasis in nude mice through CK1α. Moreover, expression of CK1α is positively correlated with HPIP in RCC samples, and also predicts poor clinical outcome-like expression of HPIP. Taken together, our data demonstrate the critical regulatory role of the HPIP-CK1α interaction in RCC, and suggest that HPIP and CK1α may be potential targets for RCC therapy.

Identifiers

PMID27694835
PMCPMC5117846
OpenAlexW2528775704

What OpenQuestion holds

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Registered trials

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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.