Evidence map›Paper›PMID 25193342›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2014

Omega-3 fatty acid is a potential preventive agent for recurrent colon cancer.

Anita Vasudevan, Yingjie Yu, Sanjeev Banerjee, James Woods, Lulu Farhana, Sindhu G Rajendra, Aamil Patel, Gregory Dyson, Edi Levi, Krishna Rao Maddipati and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

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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.

Anita VasudevanVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan.
Yingjie YuVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan. Department of Internal Medicine, Wayne State University, Detroit, Michigan.
Sanjeev BanerjeeKarmanos Cancer Institute, Wayne State University, Detroit, Michigan. Department of Pathology, Wayne State University, Detroit, Michigan.
James WoodsVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan.
Lulu FarhanaVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan. Department of Internal Medicine, Wayne State University, Detroit, Michigan.
Sindhu G RajendraVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan.
Aamil PatelVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan.
Gregory DysonKarmanos Cancer Institute, Wayne State University, Detroit, Michigan.
Edi LeviVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan. Department of Pathology, Wayne State University, Detroit, Michigan.
Krishna Rao MaddipatiKarmanos Cancer Institute, Wayne State University, Detroit, Michigan. Department of Pathology, Wayne State University, Detroit, Michigan. Lipidomics Core Facility, Wayne State University, Detroit, Michigan.
Adhip P N MajumdarVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan. Department of Internal Medicine, Wayne State University, Detroit, Michigan. Karmanos Cancer Institute, Wayne State University, Detroit, Michigan. a.majumdar@wayne.edu makkerp@karmanos.org.
Pratima Nangia-MakkerVeterans Affairs Medical Center, Wayne State University, Detroit, Michigan. Department of Internal Medicine, Wayne State University, Detroit, Michigan. Karmanos Cancer Institute, Wayne State University, Detroit, Michigan. a.majumdar@wayne.edu makkerp@karmanos.org.
The Barbara Ann Karmanos Cancer Institute · USWayne State University · US

Funding

The Aging Gut:Regulation of Cell ProliferationR01AG014343 · NIA · WAYNE STATE UNIVERSITY · PI MAJUMDAR, ADHIP P. N. · 1997 to 2011
$2.8M
Triple Quadrupole - Ion Trap Hybrid LC/MS/MS SystemS10RR027926 · NCRR · WAYNE STATE UNIVERSITY · PI MADDIPATI, KRISHNARAO · 2010 to 2010
$425k
Racial Disparity in Colorectal Cancer: Molecular MechanismsR21CA175916 · NCI · WAYNE STATE UNIVERSITY · PI MAJUMDAR, ADHIP P. N. · 2013 to 2014
$297k
Differentiation and Elimination of Chemo-surviving Colon TumorsI01BX001927 · VA · JOHN D DINGELL VA MEDICAL CENTER · PI MAJUMDAR, ADHIP P. N. · 2013 to 2016
–
BLRD VA I01 BX001927NCI NIH HHS R21 CA175916NCRR NIH HHS S10 RR027926NCRR NIH HHS S10RR027926NIA NIH HHS AG014343NIA NIH HHS R01 AG014343
6 · The paper itself

Abstract

Increasing evidence supports the contention that many malignancies, including sporadic colorectal cancer, are driven by the self-renewing, chemotherapy-resistant cancer stem/stem-like cells (CSC/CSLC), underscoring the need for improved preventive and therapeutic strategies targeting CSCs/CSLCs. Omega-3 polyunsaturated fatty acids (ω-3 PUFA), have been reported to inhibit the growth of primary tumors, but their potential as a preventive agent for recurring cancers is unexplored. The primary objectives of this investigation are (i) to examine whether eicosapentaenoic acid (EPA; one of the ω-3 PUFA) synergizes with FuOx (5-FU+Oxaliplatin), the backbone of colon cancer chemotherapy, and (ii) whether EPA by itself or in combination with conventional chemotherapy prevents the recurrence of colon cancer via eliminating/suppressing CSCs/CSLCs. FuOx-resistant (chemoresistant; CR) colon cancer cells, highly enriched in CSCs, were used for this study. Although EPA alone was effective, combination of EPA and FuOx was more potent in (i) inhibiting cell growth, colonosphere formation, and sphere-forming frequency, (ii) increasing sphere disintegration, (iii) suppressing the growth of SCID mice xenografts of CR colon cancer cells, and (iv) decreasing proinflammatory metabolites in mice. In addition, EPA + FuOx caused a reduction in CSC/CSLC population. The growth reduction by this regimen is the result of increased apoptosis as evidenced by PARP cleavage. Furthermore, increased pPTEN, decreased pAkt, normalization of β-catenin expression, localization, and transcriptional activity by EPA suggests a role for the PTEN-Akt axis and Wnt signaling in regulating this process. Our data suggest that EPA by itself or in combination with FuOx could be an effective preventive strategy for recurring colorectal cancer.

Indexed as

AnimalsAnticarcinogenic Agentsbeta CateninBiomarkers, TumorCell Line, TumorColonColonic NeoplasmsEicosapentaenoic AcidFatty Acids, Omega-3FemaleFluorouracilHumansInflammationMiceMice, SCIDNeoplasm Recurrence, LocalAnticarcinogenic Agentsbeta CateninBiomarkers, TumorEicosapentaenoic AcidFatty Acids, Omega-3FluorouracilOrganoplatinum CompoundsOxaliplatin

Identifiers

PMID25193342
PMCPMC4221533
OpenAlexW2088596997

What OpenQuestion holds

Textmetadata
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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.