Evidence map›Paper›PMID 28032857›Full record

ArticleCell death & disease2016

Heme oxygenase-1 in the forefront of a multi-molecular network that governs cell-cell contacts and filopodia-induced zippering in prostate cancer.

Alejandra V Paez, Carla Pallavicini, Federico Schuster, Maria Pia Valacco, Jimena Giudice, Emiliano G Ortiz, Nicolás Anselmino, Estefania Labanca, Maria Binaghi, Marcelo Salierno and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.1field-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

32 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. [Antitumor component-Ι inNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Prostate cancer in omics era.Cancer cell international · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Toxicological research · 2021
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. 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

18 authors at 6 institutions in 2 countries.

Alejandra V PaezDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Carla PallaviciniDepartment of Physics, FCEN, University of Buenos Aires, IFIBA-CONICET, Buenos Aires, Argentina.
Federico SchusterDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Maria Pia ValaccoDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Jimena GiudiceDepartment of Cell Biology and Physiology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Emiliano G OrtizDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Nicolás AnselminoDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Estefania LabancaDepartment of Genitourinary Medical Oncology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Maria BinaghiDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Marcelo SaliernoDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Marcelo A MartíDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Javier H CotignolaDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Anna Woloszynska-ReadPharmacology and Therapeutics Department, Roswell Park Cancer Institute, Buffalo, NY, USA.
Luciana BrunoDepartment of Physics, FCEN, University of Buenos Aires, IFIBA-CONICET, Buenos Aires, Argentina.
Valeria LeviDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Nora NavoneDepartment of Genitourinary Medical Oncology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Elba S VazquezDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
Geraldine GueronDepartment of Biological Chemistry, School of Sciences, FCEN, University of Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina.
University of Buenos Aires · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARInstituto de Química y Fisicoquímica Biológicas · ARThe University of Texas MD Anderson Cancer Center · USRoswell Park Comprehensive Cancer Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Targeting Tumor Microenvironment-Induced Therapy Resistance in Prostate Cancer Bone MetastasisP50CA140388 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOGOTHETIS, CHRISTOPHER J., THOMPSON, TIMOTHY CHARLES · 2009 to 2022
$23.4M
NCI NIH HHS P50 CA140388
6 · The paper itself

Abstract

Prostate cancer (PCa) cells display abnormal expression of cytoskeletal proteins resulting in an augmented capacity to resist chemotherapy and colonize distant organs. We have previously shown that heme oxygenase 1 (HO-1) is implicated in cell morphology regulation in PCa. Here, through a multi 'omics' approach we define the HO-1 interactome in PCa, identifying HO-1 molecular partners associated with the integrity of the cellular cytoskeleton. The bioinformatics screening for these cytoskeletal-related partners reveal that they are highly misregulated in prostate adenocarcinoma compared with normal prostate tissue. Under HO-1 induction, PCa cells present reduced frequency in migration events, trajectory and cell velocity and, a significant higher proportion of filopodia-like protrusions favoring zippering among neighboring cells. Moreover forced expression of HO-1 was also capable of altering cell protrusions in transwell co-culture systems of PCa cells with MC3T3 cells (pre-osteoblastic cell line). Accordingly, these effects were reversed under siHO. Transcriptomics profiling evidenced significant modulation of key markers related to cell adhesion and cell-cell communication under HO-1 induction. The integration from our omics-based research provides a four molecular pathway foundation (ANXA2/HMGA1/POU3F1; NFRSF13/GSN; TMOD3/RAI14/VWF; and PLAT/PLAU) behind HO-1 regulation of tumor cytoskeletal cell compartments. The complementary proteomics and transcriptomics approaches presented here promise to move us closer to unravel the molecular framework underpinning HO-1 involvement in the modulation of cytoskeleton pathways, pushing toward a less aggressive phenotype in PCa.

Indexed as

Gene Regulatory NetworksAnimalsCell CommunicationCell Line, TumorCell MovementCoculture TechniquesCrystallography, X-RayCulture Media, ConditionedCytoskeletonGene Expression Regulation, NeoplasticHeme Oxygenase-1HumansMaleMiceOligonucleotide Array Sequence AnalysisProstatic NeoplasmsCulture Media, ConditionedHeme Oxygenase-1

Identifiers

PMID28032857
PMCPMC5261017
OpenAlexW2565442619

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.