Evidence map›Paper›PMID 25558447›Full record

ArticleBBA clinical2014

Elevation of serum fortilin levels is specific for apoptosis and signifies cell death in vivo.

Patuma Sinthujaroen, Nattaporn Wanachottrakul, Decha Pinkaew, John R Petersen, Amornrat Phongdara, Melinda Sheffield-Moore, Ken Fujise

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in BBA clinical, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05490953 (Enhancing Effect on Tumour Apoptosis With the Combined Use of Pentoxifylline Plus Chemotherapeutical Agents in Pediatrics and AYA Patients With Hodgkin´s Lymphoma), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 33% 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.

NCT05490953 phase4unknown statusnot on this mapstarted 2022, after this paper: background citation

Enhancing Effect on Tumour Apoptosis With the Combined Use of Pentoxifylline Plus Chemotherapeutical Agents in Pediatrics and AYA Patients With Hodgkin´s Lymphoma

TypeinterventionalSponsorUniversity of GuadalajaraRan2022 to 2024Enrolled30ConditionsHodgkin LymphomaArmsPentoxifylline, Placebo
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. High Plasma Levels of Fortilin in Patients with Coronary Artery Disease.International journal of molecular sciences · 2022
    Article
  7. Article
  8. Article
  9. Reduced Nhe1 (NaHypertension (Dallas, Tex. : 1979) · 2020
    Article
  10. NaNature communications · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Review
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

7 authors at 2 institutions in 2 countries.

Patuma SinthujaroenDivision of Cardiology, University of Texas Medical Branch at Galveston, TX 77555, USA ; Center for Genomics and Bioinformatics Research, Faculty of Science, Prince of Songkla University, Thailand.
Nattaporn WanachottrakulDivision of Cardiology, University of Texas Medical Branch at Galveston, TX 77555, USA.
Decha PinkaewDivision of Cardiology, University of Texas Medical Branch at Galveston, TX 77555, USA.
John R PetersenDepartment of Pathology, University of Texas Medical Branch at Galveston, TX 77555, USA.
Amornrat PhongdaraCenter for Genomics and Bioinformatics Research, Faculty of Science, Prince of Songkla University, Thailand.
Melinda Sheffield-MooreDivision of Endocrinology and Metabolism within the Department of Internal Medicine, University of Texas Medical Branch at Galveston, TX 77555, USA.
Ken FujiseDivision of Cardiology, University of Texas Medical Branch at Galveston, TX 77555, USA ; Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, TX 77555, USA.
The University of Texas Medical Branch at Galveston · USPrince of Songkla University · TH

Funding

UTMB Clinical and Translational Science AwardUL1TR000071 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BRASIER, ALLAN R. · 2012 to 2014
$14.4M
Fortilin, p53, and atherosclerosisR01HL117247 · NHLBI · UNIVERSITY OF WASHINGTON · PI CHEN, SHIYOU, FUJISE, KEN · 2013 to 2023
$4.7M
Novel mechanism of smooth muscle phenotypic modulation and vascular remodelingR01HL119053 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHEN, SHIYOU · 2014 to 2023
$3.8M
Nutrition and Anabolic Interventions in Cancer CachexiaR01CA127971 · NCI · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SHEFFIELD-MOORE, MELINDA · 2008 to 2014
$1.8M
NCATS NIH HHS UL1 TR000071NCI NIH HHS R01 CA127971NHLBI NIH HHS R01 HL117247NHLBI NIH HHS R01 HL119053
6 · The paper itself

Abstract

backgroundBillions of cells undergo apoptosis each day in the average normal adult. The ability to readily assess the degree of apoptosis in human diseases is hampered by the lack of sensitive and specific serum biomarkers of apoptosis. Fortilin is a novel prosurvival molecule that protects cells against various noxious stimuli. While fortilin is secreted into the extracellular space under certain conditions, the relationship between the serum concentration of fortilin and the presence and extent of apoptosis in vivo remains unknown. METHODS &

resultsUsing a newly developed fortilin ELISA system, we show here that fortilin exists in the normal human and mouse circulation. We further demonstrate that fortilin serum levels are significantly elevated in patients with solid cancer, in response to anti-cancer chemo- or radiation therapy. The elevation of fortilin serum levels is more robust and sensitive than that of such previously-reported serum biomarkers of apoptosis as fragmented cytokeratin-18, cytochrome c, and nucleosomal DNA. In addition, targeted apoptotic liver damage induced by Jo2 anti-Fas (CD95) antibody consistently and significantly increased serum fortilin levels in C57BL/6J mice. Finally, when challenged by anti-human-Fas IgM antibody, Jurkat leukemic T cells apoptosed and released fortilin into the medium before plasma membrane integrity was compromised.

conclusionsTaken together, these data suggest that serum fortilin levels reflect the degree and extent of apoptosis occurring in vivo. GENERAL SIGNIFICANCE: Fortilin is a viable serum biomarker of in vivo apoptosis and can be utilized to noninvasively assess the status of in vivo apoptosis in humans.

Indexed as

ApoptosisBiomarkerFortilinProgrammed Cell Death

Identifiers

PMID25558447
PMCPMC4280861
OpenAlexW2079035108

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.