Evidence map›Paper›PMID 26110425›Full record

ArticlePloS one2015

Identification of CREB3L1 as a Biomarker Predicting Doxorubicin Treatment Outcome.

Bray Denard, Andrea Pavia-Jimenez, Weina Chen, Noelle S Williams, Harris Naina, Robert Collins, James Brugarolas, Jin Ye

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Uptake of HDL-cholesterol contributes to lipid accumulation in clear cell renal cell carcinoma.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Article
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  15. Advances in delivery systems for doxorubicin.Journal of nanomedicine & nanotechnology · 2018
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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

8 authors at 1 institution in 1 country.

Bray DenardDepartment of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
Andrea Pavia-JimenezDepartment of Internal Medicine, Hematology-Oncology Division, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America; Department of Developmental Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
Weina ChenDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
Noelle S WilliamsDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
Harris NainaDepartment of Internal Medicine, Hematology-Oncology Division, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
Robert CollinsDepartment of Internal Medicine, Hematology-Oncology Division, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
James BrugarolasDepartment of Internal Medicine, Hematology-Oncology Division, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America; Department of Developmental Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America; Kidney Cancer Program in Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
Jin YeDepartment of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States of America.
The University of Texas Southwestern Medical Center · US

Funding

TRANSCRIPTIONAL REGULATION OF LDL RECEPTOR PROMOTERP01HL020948 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI GOLDSTEIN, JOSEPH L · 1985 to 2021
$103.1M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
Regulated Intramembrane Proteolysis of CREB3L1 in Innate Antiviral ResponseR01AI090119 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI YE, JIN · 2010 to 2014
$1.9M
Proteolytic activation of CREB3L1 in treating cancers and tissue fibrosisR01GM116106 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI YE, JIN · 2015 to 2018
$1.6M
Infectious Diseases Training ProgramT32AI070116 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI PERL, TRISH M. · 2007 to 2017
$1.1M
NCI NIH HHS P30 CA142543NHLBI NIH HHS HL20948NHLBI NIH HHS P01 HL020948NIAID NIH HHS AI 090119NIAID NIH HHS AI70116NIAID NIH HHS R01 AI090119NIAID NIH HHS T32 AI070116NIGMS NIH HHS R01 GM116106
6 · The paper itself

Abstract

backgroundDoxorubicin has been shown to inhibit proliferation of cancer cells through proteolytic activation of CREB3L1 (cAMP response element binding protein 3-like 1), a transcription factor synthesized as a membrane-bound precursor. Upon doxorubicin treatment, CREB3L1 is cleaved so that the N-terminal domain of the protein can reach the nucleus where it activates transcription of genes that inhibit cell proliferation. These results suggest that the level of CREB3L1 in cancer cells may determine their sensitivity to doxorubicin.

methodsMice transplanted with 6 lines of renal cell carcinoma (RCC) were injected with doxorubicin to observe the effect of the chemotherapy on tumor growth. Immunohistochemistry and bioinformatics analyses were performed to compare CREB3L1 levels in types of cancer known to respond to doxorubicin versus those resistant to doxorubicin.

resultsHigher levels of CREB3L1 protein are correlated with increased doxorubicin sensitivity of xenograft RCC tumors (p = 0.017 by Pearson analysis). From patient tumor biopsies we analyzed, CREB3L1 was expressed in 19% of RCC, which is generally resistant to doxorubicin, but in 70% of diffuse large B-cell lymphoma that is sensitive to doxorubicin. Doxorubicin is used as the standard treatment for cancers that express the highest levels of CREB3L1 such as osteosarcoma and malignant fibrous histiocytoma but is not generally used to treat those that express the lowest levels of CREB3L1 such as RCC.

conclusionIdentification of CREB3L1 as the biomarker for doxorubicin sensitivity may markedly improve the doxorubicin response rate by applying doxorubicin only to patients with cancers expressing CREB3L1.

Indexed as

AnimalsAntineoplastic AgentsBiomarkersCarcinoma, Renal CellCell Line, TumorCell ProliferationCyclic AMP Response Element-Binding ProteinDoxorubicinFemaleHumansKidney NeoplasmsLymphoma, Large B-Cell, DiffuseMiceNeoplasm TransplantationNerve Tissue ProteinsPrognosisAntineoplastic AgentsBiomarkersCreb3l1 protein, mouseCyclic AMP Response Element-Binding ProteinDoxorubicinNerve Tissue Proteins

Identifiers

PMID26110425
PMCPMC4482141
OpenAlexW1525702510

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.