Evidence map›Paper›PMID 28067315›Full record

ArticleScientific reports2017

KANK1 inhibits cell growth by inducing apoptosis through regulating CXXC5 in human malignant peripheral nerve sheath tumors.

Zhibin Cui, Yingjia Shen, Kenny H Chen, Suresh K Mittal, Jer-Yen Yang, GuangJun Zhang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Signal integrator function of CXXC5 in Cancer.Cell communication and signaling : CCS · 2025
    Review
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  15. Kank1 and Ki67 expression are associated with poor prognosis in human pulmonary adenocarcinoma.International journal of clinical and experimental pathology · 2020
    Article
  16. CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling.Journal of cellular and molecular medicine · 2019
    Review
  17. Article
  18. Identification ofOncotarget · 2018
    Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Zhibin CuiDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana, United States.
Yingjia ShenA316 Environment and Ecology Building, Xiamen, Fujian 361102, China.
Kenny H ChenDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana, United States.
Suresh K MittalDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana, United States.
Jer-Yen YangPurdue University Center for Cancer Research, West Lafayette, Indiana, United States.
GuangJun ZhangDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana, United States.
Purdue University West Lafayette · USCenter for Cancer Research · USInstitute of Urban Environment · CN

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI Andrea L Kasinski · 1985 to 2026
$43.4M
NCI NIH HHS P30 CA023168
6 · The paper itself

Abstract

Malignant peripheral nerve sheath tumors (MPNSTs) are a type of rare sarcomas with a poor prognosis due to its highly invasive nature and limited treatment options. Currently there is no targeted-cancer therapy for this type of malignancy. Thus, it is important to identify more cancer driver genes that may serve as targets of cancer therapy. Through comparative oncogenomics, we have found that KANK1 was a candidate tumor suppressor gene (TSG) for human MPNSTs. Although KANK1 is known as a cytoskeleton regulator, its tumorigenic function in MPNSTs remains largely unknown. In this study, we report that restoration of KANK1 in human MPNST cells inhibits cell growth both in human cell culture and xenograft mice by increasing apoptosis. Consistently, knockdown of KANK1 in neurofibroma cells promoted cell growth. Using RNA-seq analysis, we identified CXXC5 and other apoptosis-related genes, and demonstrated that CXXC5 is regulated by KANK1. Knockdown of CXXC5 was found to diminish KANK1-induced apoptosis in MPNST cells. Thus, KANK1 inhibits MPNST cell growth though CXXC5 mediated apoptosis. Our results suggest that KANK1 may function as a tumor suppressor in human MPNSTs, and thus it may be useful for targeted therapy.

Indexed as

ApoptosisGene Expression Regulation, NeoplasticAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell Line, TumorCell ProliferationCytoskeletal ProteinsDNA-Binding ProteinsGene DosageGene Knockdown TechniquesHumansMice, Inbred NODMice, SCIDNerve Sheath NeoplasmsTranscription FactorsAdaptor Proteins, Signal TransducingCarrier ProteinsCXXC5 protein, humanCytoskeletal ProteinsDNA-Binding ProteinsKANK1 protein, humanTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID28067315
PMCPMC5220314
OpenAlexW2570682266

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.