Evidence map›Paper›PMID 25628921›Full record

ArticleAmerican journal of cancer research2015

Dovitinib (TKI258), a multi-target angiokinase inhibitor, is effective regardless of KRAS or BRAF mutation status in colorectal cancer.

Choong-Kun Lee, Myung Eun Lee, Won Suk Lee, Jeong Min Kim, Kyu Hyun Park, Tae Soo Kim, Kang Young Lee, Joong Bae Ahn, Hyun Cheol Chung, Sun Young Rha

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.4field-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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Anti-Angiogenic Therapy: Current Challenges and Future Perspectives.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Observational
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

10 authors at 2 institutions in 1 country.

Choong-Kun LeeDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine Seoul, Korea.
Myung Eun LeeBrain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Won Suk LeeBrain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Jeong Min KimBrain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Kyu Hyun ParkBrain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Tae Soo KimBrain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Kang Young LeeDepartment of Surgery, Gangnam Severance Hospital, Yonsei University College of Medicine Seoul, Korea.
Joong Bae AhnDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine Seoul, Korea ; Brain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Hyun Cheol ChungDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine Seoul, Korea ; Brain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Sun Young RhaDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine Seoul, Korea ; Brain Korea 21 Project for Medical Science, Institute for Cancer Research, Yonsei University College of Medicine Seoul, Korea.
Yonsei University · KRGangnam Severance Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe aimed to determine whether KRAS and BRAF mutant colorectal cancer (CRC) cells exhibit distinct sensitivities to the multi-target angiokinase inhibitor, TKI258 (dovitinib). MATERIALS AND

methodsWe screened 10 CRC cell lines by using receptor tyrosine kinase (RTK) array to identify activated RTKs. MTT assays, anchorage-independent colony-formation assays, and immunoblotting assays were performed to evaluate the in vitro anti-tumor effects of TKI258. In vivo efficacy study followed by pharmacodynamic evaluation was done.

resultsFibroblast Growth Factor Receptor 1 (FGFR1) and FGFR3 were among the most highly activated RTKs in CRC cell lines. In in vitro assays, the BRAF mutant HT-29 cells were more resistant to the TKI258 than the KRAS mutant LoVo cells. However, in xenograft assays, TKI258 equally delayed the growth of tumors induced by both cell lines. TUNEL assays showed that the apoptotic index was unchanged following TKI258 treatment, but staining for Ki-67 and CD31 was substantially reduced in both xenografts, implying an anti-angiogenic effect of the drug. TKI258 treatment was effective in delaying CRC tumor growth in vivo regardless of the KRAS and BRAF mutation status.

conclusionsOur results identify FGFRs as potential targets in CRC treatment and suggest that combined targeting of multiple RTKs with TKI258 might serve as a novel approach to improve outcome of patients with CRC.

Indexed as

BRAFColorectal cancerDovitinib (TKI258)FGFRKRASmulti-target angiokinase inhibitor

Identifiers

PMID25628921
PMCPMC4300687
OpenAlexW1518173575

What OpenQuestion holds

Textmetadata
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.