Evidence map›Paper›PMID 18388920›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2008

Therapeutic molecular targeting of 15-lipoxygenase-1 in colon cancer.

Yuanqing Wu, Bingliang Fang, Xiulan Q Yang, Li Wang, Dongning Chen, Victor Krasnykh, Bing Z Carter, Jeffrey S Morris, Imad Shureiqi

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Lipoxygenases at the Intersection of Infection and Carcinogenesis.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. ALOX15 as a suppressor of inflammation and cancer: Lost in the link.Prostaglandins & other lipid mediators · 2017
    Review
  8. 15-Lipoxygenase-1 suppression of colitis-associated colon cancer through inhibition of the IL-6/STAT3 signaling pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  9. Mammalian lipoxygenases and their biological relevance.Biochimica et biophysica acta · 2015
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Profiling lipoxygenase metabolism in specific steps of colorectal tumorigenesis.Cancer prevention research (Philadelphia, Pa.) · 2010
    Article
  20. Article
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

9 authors at 1 institution in 1 country.

Yuanqing WuDepartment of Clinical Cancer Prevention, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030-4009, USA.
Bingliang Fang
Xiulan Q Yang
Li Wang
Dongning Chen
Victor Krasnykh
Bing Z Carter
Jeffrey S Morris
Imad Shureiqi
The University of Texas MD Anderson Cancer Center · US

Funding

Molecular Targeting of 15-Lipoxygenase-1 in Colon CancerR01CA104278 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHUREIQI, IMAD · 2004 to 2007
$1.0M
NCI NIH HHS R01 CA104278
6 · The paper itself

Abstract

Molecular targeting for apoptosis induction is being developed for better treatment of cancer. Downregulation of 15-lipoxygenase-1 (15-LOX-1) is linked to colorectal tumorigenesis. Re-expression of 15-LOX-1 in cancer cells by pharmaceutical agents induces apoptosis. Antitumorigenic agents can also induce apoptosis via other molecular targets. Whether restoring 15-LOX-1 expression in cancer cells is therapeutically sufficient to inhibit colonic tumorigenesis remains unknown. We tested this question using an adenoviral delivery system to express 15-LOX-1 in in vitro and in vivo models of colon cancer. We found that (i) the adenoviral vector 5/3 fiber modification enhanced 15-LOX-1 gene transduction in various colorectal cancer cell lines, (ii) the adenoviral vector delivery restored 15-LOX-1 expression and enzymatic activity to therapeutic levels in colon cancer cell lines, and (iii) 15-LOX-1 expression downregulated the expression of the antiapoptotic proteins X-linked inhibitor of apoptosis protein (XIAP) and BcL-XL, activated caspase-3, triggered apoptosis, and inhibited cancer cell survival in vitro and the growth of colon cancer xenografts in vivo. Thus, selective molecular targeting of 15-LOX-1 expression is sufficient to re-establish apoptosis in colon cancer cells and inhibit tumorigenesis. These data provide the rationale for further development of therapeutic strategies to target 15-LOX-1 molecularly for treating colonic tumorigenesis.

Indexed as

Gene Expression Regulation, NeoplasticAdenoviridaeAnimalsAntineoplastic AgentsApoptosisArachidonate 15-Lipoxygenasebcl-X ProteinCaspase 3Colonic NeoplasmsGenetic TherapyGene Transfer TechniquesHumansMiceNeoplasm TransplantationX-Linked Inhibitor of Apoptosis ProteinAntineoplastic AgentsArachidonate 15-Lipoxygenasebcl-X ProteinCaspase 3XIAP protein, humanX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID18388920
PMCPMC2377397
OpenAlexW2089070183

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.