Evidence map›Paper›PMID 28569777›Full record

ArticleCell death & disease2017

The novel hypoxia-inducible factor-1α inhibitor IDF-11774 regulates cancer metabolism, thereby suppressing tumor growth.

Hyun Seung Ban, Bo-Kyung Kim, Hongsub Lee, Hwan Mook Kim, Dipesh Harmalkar, Miso Nam, Song-Kyu Park, Kiho Lee, Joon-Tae Park, Inhyub Kim and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Interaction of HIF-1a with various cell death pathways in tumor immune microenvironment (TIME).Apoptosis : an international journal on programmed cell death · 2026
    Pooled it
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  15. Targeted Cancer Therapy-on-A-Chip.Advanced healthcare materials · 2024
    Review
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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

13 authors at 6 institutions in 1 country.

Hyun Seung BanMetabolic Regulation Research Center, KRIBB, Daejeon 305-806, Korea.
Bo-Kyung KimPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 305-806, Korea.
Hongsub LeeDrug Discovery Team, ILDONG Pharmaceutical Co. Ltd, Hwaseong 445-811, Kyungi-do, Korea.
Hwan Mook KimCollege of Pharmacy, Gachon University, Incheon 406-840, Korea.
Dipesh HarmalkarCollege of Pharmacy, Dongguk University-Seoul, Goyang 410-820, Korea.
Miso NamIntegrated Metabolomics Research Group, Western Seoul Center, Korea Basic Science Institute, Seoul, Korea.
Song-Kyu ParkCollege of Pharmacy, Korea University, Sejong City 30019, Korea.
Kiho LeeCollege of Pharmacy, Korea University, Sejong City 30019, Korea.
Joon-Tae ParkDrug Discovery Team, ILDONG Pharmaceutical Co. Ltd, Hwaseong 445-811, Kyungi-do, Korea.
Inhyub KimPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 305-806, Korea.
Kyeong LeeCollege of Pharmacy, Dongguk University-Seoul, Goyang 410-820, Korea.
Geum-Sook HwangIntegrated Metabolomics Research Group, Western Seoul Center, Korea Basic Science Institute, Seoul, Korea.
Misun WonPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 305-806, Korea.
Korea Research Institute of Bioscience and Biotechnology · KRDongguk University · KRKorea Basic Science Institute · KRKorea University · KRKyungdong Pharmaceutical (South Korea) · KRGachon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIF-1 is associated with poor prognoses and therapeutic resistance in cancer patients. We previously developed a novel hypoxia-inducible factor (HIF)-1 inhibitor, IDF-11774, a clinical candidate for cancer therapy. We also reported that IDF-1174 inhibited HSP70 chaperone activity and suppressed accumulation of HIF-1α. In this study, IDF-11774 inhibited the accumulation of HIF-1α in vitro and in vivo in colorectal carcinoma HCT116 cells under hypoxic conditions. Moreover, IDF-11774 treatment suppressed angiogenesis of cancer cells by reducing the expression of HIF-1 target genes, reduced glucose uptake, thereby sensitizing cells to growth under low glucose conditions, and decreased the extracellular acidification rate (ECAR) and oxygen consumption rate of cancer cells. Metabolic profiling of IDF-11774-treated cells revealed low levels of NAD

Indexed as

Gene Expression Regulation, NeoplasticAdamantaneAnimalsAntineoplastic AgentsCell ProliferationColorectal NeoplasmsCyclic AMPFemaleGlucoseGlycolysisHCT116 CellsHumansHypoxia-Inducible Factor 1, alpha SubunitLactic AcidMiceMice, NudeAdamantaneAntineoplastic AgentsCyclic AMPGlucoseHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitIDF-11774KRAS protein, humanLactic AcidMTOR protein, humanNADPiperazinesProto-Oncogene Proteins p21(ras)PTEN PhosphohydrolasePTEN protein, humanTOR Serine-Threonine KinasesVHL protein, humanVon Hippel-Lindau Tumor Suppressor Protein

Identifiers

PMID28569777
PMCPMC5520894
OpenAlexW2621296296

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.