Evidence map›Paper›PMID 26325365›Full record

ArticlemAbs2015

Anticancer activity of TTAC-0001, a fully human anti-vascular endothelial growth factor receptor 2 (VEGFR-2/KDR) monoclonal antibody, is associated with inhibition of tumor angiogenesis.

Dong Geon Kim, Younggeon Jin, Juyoun Jin, Heekyoung Yang, Kyeung Min Joo, Weon Sup Lee, Sang Ryeol Shim, Sung-Woo Kim, Jinsang Yoo, Sang Hoon Lee and 2 more

Open access · goldAbstract read
In one paragraph

Article in mAbs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% 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.

  1. NMR mapping of the highly flexible regions ofJournal of biomolecular NMR · 2020
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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

12 authors at 2 institutions in 1 country.

Dong Geon Kima Institute for Refractory Cancer Research, Research Institute for Future Medicine, Samsung Medical Center ; Seoul 06351 , Korea.
Younggeon Jina Institute for Refractory Cancer Research, Research Institute for Future Medicine, Samsung Medical Center ; Seoul 06351 , Korea.
Juyoun Jina Institute for Refractory Cancer Research, Research Institute for Future Medicine, Samsung Medical Center ; Seoul 06351 , Korea.
Heekyoung Yanga Institute for Refractory Cancer Research, Research Institute for Future Medicine, Samsung Medical Center ; Seoul 06351 , Korea.
Kyeung Min Jooa Institute for Refractory Cancer Research, Research Institute for Future Medicine, Samsung Medical Center ; Seoul 06351 , Korea.
Weon Sup Leee PharmAbcine; Inc., Daejeon Bioventure Town ; Daejeon 34054 , Korea.
Sang Ryeol Shime PharmAbcine; Inc., Daejeon Bioventure Town ; Daejeon 34054 , Korea.
Sung-Woo Kime PharmAbcine; Inc., Daejeon Bioventure Town ; Daejeon 34054 , Korea.
Jinsang Yooe PharmAbcine; Inc., Daejeon Bioventure Town ; Daejeon 34054 , Korea.
Sang Hoon Leef Bio Division, Hanwha Chemical ; Seoul 04541 , Korea.
Jin-San Yooe PharmAbcine; Inc., Daejeon Bioventure Town ; Daejeon 34054 , Korea.
Do-Hyun Nama Institute for Refractory Cancer Research, Research Institute for Future Medicine, Samsung Medical Center ; Seoul 06351 , Korea.
Samsung Medical Center · KRDongwha Pharm (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular endothelial growth factor (VEGF) and its receptors are considered the primary cause of tumor-induced angiogenesis. Specifically, VEGFR-2/kinase insert domain receptor (KDR) is part of the major signaling pathway that plays a significant role in tumor angiogenesis, which is associated with the development of various types of tumor and metastasis. In particular, KDR is involved in tumor angiogenesis as well as cancer cell growth and survival. In this study, we evaluated the therapeutic potential of TTAC-0001, a fully human antibody against VEGFR-2/KDR. To assess the efficacy of the antibody and pharmacokinetic (PK) relationship in vivo, we tested the potency of TTAC-0001 in glioblastoma and colorectal cancer xenograft models. Antitumor activity of TTAC-0001 in preclinical models correlated with tumor growth arrest, induction of tumor cell apoptosis, and inhibition of angiogenesis. We also evaluated the combination effect of TTAC-0001 with a chemotherapeutic agent in xenograft models. We were able to determine the relationship between PK and the efficacy of TTAC-0001 through in vivo single-dose PK study. Taken together, our data suggest that targeting VEGFR-2 with TTAC-0001 could be a promising approach for cancer treatment.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsApoptosisArea Under CurveCell Line, TumorColorectal NeoplasmsGlioblastomaHCT116 CellsHT29 CellsHumansMCF-7 CellsMice, Inbred BALB CMice, NudeNeoplasmsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsolinvacimabVascular Endothelial Growth Factor Receptor-2colorectal cancerfully human neutralizing antibody, angiogenesis inhibitorglioblastomapharmacokineticsTTAC-0001tumor growth inhibitionVEGF signaling

Identifiers

PMID26325365
PMCPMC4966428
OpenAlexW2155694671

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.