Evidence map›Paper›PMID 27083053›Full record

ArticleOncotarget2016

Necrosis-inducing peptide has the beneficial effect on killing tumor cells through neuropilin (NRP-1) targeting.

Ji-Young Kim, Ji-Hae Han, Geon Park, Young-Woo Seo, Cheol-Won Yun, Byung-Chul Lee, Jeehyeon Bae, Ae Ran Moon, Tae-Hyoung Kim

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Ji-Young KimDepartment of Biochemistry, Chosun University School of Medicine, Dong-Gu, Gwang-Ju, Korea.
Ji-Hae HanDepartment of Biochemistry, Chosun University School of Medicine, Dong-Gu, Gwang-Ju, Korea.
Geon ParkDepartment of Laboratory Medicine, Chosun University School of Medicine, Dong-Gu, Gwang-Ju, Korea.
Young-Woo SeoKorea Basic Science Institute Gwang-Ju Center, Chonnam National University, Buk-Gu, Gwang-Ju, Korea.
Cheol-Won YunSchool of Life Science and Biotechnology, Korea University, Seoul, Korea.
Byung-Chul LeeGenoflux. Co., Ltd., Sejong City, Korea.
Jeehyeon BaeSchool of Pharmacy, Chung-Ang University, Dongjak-Gu, Seoul, Korea.
Ae Ran MoonDepartment of Biochemistry, Chosun University School of Medicine, Dong-Gu, Gwang-Ju, Korea.
Tae-Hyoung KimDepartment of Biochemistry, Chosun University School of Medicine, Dong-Gu, Gwang-Ju, Korea.
Chosun University · KRChonnam National University · KRChung-Ang University · KRKorea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The therapeutic efficacy of most anti-cancer drugs depends on their apoptosis-inducing abilities. Previously, we showed that a peptide containing the mitochondrial targeting domain (MTD) found in Noxa, a BH-3 only protein of Bcl-2 family, induces necrosis. Here, a fusion peptide of neuropilin-1 (NRP-1) targeting peptide and MTD peptide, designated tumor homing motif 17:MTD (TU17:MTD), was found to induce necrosis in cancer cells in vitro and to cause the regression of tumors when intravenously injected into mice bearing subcutaneous CT26 colorectal carcinoma tumors. The necrosis within tumor tissues was evident upon administering TU17:MTD. TU17:MTD penetrated into tumor cells by targeting to Neuropilin-1, which could be blocked by anti-NRP-1 antibody. The efficacy of TU17:MTD on tumor regression was higher than that of TU17:D(KLAKLAK)2, a fusion peptide of NRP-1 targeting peptide and a pro-apoptotic peptide. The necrotic cell death within tumor tissues was evident at day 1 after administering TU17:MTD systemically. Transplanted subcutaneous substantially reduced in size within two weeks and 5 days, respectively, with no apparent side effects. Together, these results propose that the pro-necrotic peptide MTD may present an alternative approach for development of targeted anti-cancer agents.

Indexed as

AnimalsColorectal NeoplasmsHumansMaleMiceMice, Inbred BALB CMolecular Targeted TherapyNecrosisNeuropilin-1Peptide FragmentsProtein DomainsProto-Oncogene Proteins c-bcl-2Recombinant Fusion ProteinsTumor Cells, CulturedXenograft Model Antitumor AssaysNeuropilin-1Peptide FragmentsPMAIP1 protein, humanProto-Oncogene Proteins c-bcl-2Recombinant Fusion Proteinsmitochondrial targeting domainnecrosisNoxaNRP-1pro-necrotic peptide

Identifiers

PMID27083053
PMCPMC5078025
OpenAlexW2340938824

What OpenQuestion holds

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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.