Evidence map›Paper›PMID 18594009›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2008

Honokiol suppresses survival signals mediated by Ras-dependent phospholipase D activity in human cancer cells.

Avalon Garcia, Yang Zheng, Chen Zhao, Alfredo Toschi, Judy Fan, Natalie Shraibman, H Alex Brown, Dafna Bar-Sagi, David A Foster, Jack L Arbiser

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06566443 (Phase I Trial Evaluating the Safety of the Dietary Supplement Honokiol in Early-Stage Resectable Non-Small Cell Lung Cancer), which is not on this map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.4field-weighted citation impact, top 3% 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.

NCT06566443 phase1recruitingnot on this mapstarted 2025, after this paper: background citation

Phase I Trial Evaluating the Safety of the Dietary Supplement Honokiol in Early-Stage Resectable Non-Small Cell Lung Cancer

TypeinterventionalSponsorThe Methodist Hospital Research InstituteRan2025 to 2027Enrolled15ConditionsCarcinoma, Non-Small-Cell LungArmsHonokiol
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Role of natural compounds in preventing and treating breast cancer.Frontiers in bioscience (Scholar edition) · 2020
    Article
  5. Review
  6. Review
  7. Review
  8. Honokiol is a FOXM1 antagonist.Cell death & disease · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Cellular and physiological roles for phospholipase D1 in cancer.The Journal of biological chemistry · 2014
    Review
  16. Review
  17. Review
  18. Article
  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

10 authors at 5 institutions in 1 country.

Avalon GarciaDepartment of Biological Sciences, Hunter College of The City University of New York, New York 10021, USA.
Yang Zheng
Chen Zhao
Alfredo Toschi
Judy Fan
Natalie Shraibman
H Alex Brown
Dafna Bar-Sagi
David A Foster
Jack L Arbiser
City University of New York · USHunter College · USNew York University · USEmory University · USVanderbilt University · US

Funding

TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
WILD TYPE &MUTANT P53 INTERACTIONS WITH HIV LTR DNAG12RR003037 · NCRR · HUNTER COLLEGE · PI DOTTIN, ROBERT P · 1985 to 2011
$27.6M
UBIQUITINATED PROTEIN DEGRADATION AND NEURODEGENERATIONS06GM060654 · NIGMS · HUNTER COLLEGE · PI LUINE, VICTORIA N · 2000 to 2011
$21.2M
Role of phospholipase D in tumorigenesisR01CA046677 · NCI · HUNTER COLLEGE · PI FOSTER, DAVID A · 1997 to 2014
$3.6M
UV light and the cutaneous neurosensory systemP30AR042687 · NIAMS · EMORY UNIVERSITY · PI CAUGHMAN, STEWART W · 1994 to 2003
$2.5M
PHOSPHOLIPASE ACTIVATION BY G-PROTEIN-LINKED RECEPTORSR01GM058516 · NIGMS · VANDERBILT UNIVERSITY · PI BROWN, ALEX · 2000 to 2004
$1.2M
BASIS FOR TRANSFORMATION BY FUJINAMI SARCOMA VIRUSR29CA046677 · NCI · HUNTER COLLEGE · PI FOSTER, DAVID A · 1989 to 1993
–
NCI NIH HHS CA46677NCI NIH HHS P50 CA098131NCI NIH HHS P50CA098131NCI NIH HHS R01 CA046677NCRR NIH HHS G12 RR003037NCRR NIH HHS RR-03037NIAMS NIH HHS AR02030NIAMS NIH HHS AR42687NIAMS NIH HHS P30 AR042687NIGMS NIH HHS GM58516NIGMS NIH HHS GM60654NIGMS NIH HHS R01 GM058516NIGMS NIH HHS S06 GM060654
6 · The paper itself

Abstract

purposeElevated phospholipase D (PLD) activity provides a survival signal in several human cancer cell lines and suppresses apoptosis when cells are subjected to the stress of serum withdrawal. Thus, targeting PLD survival signals has potential to suppress survival in cancer cells that depend on PLD for survival. Honokiol is a compound that suppresses tumor growth in mouse models. The purpose of this study was to investigate the effect of honokiol on PLD survival signals and the Ras dependence of these signals. EXPERIMENTAL

designThe effect of honokiol upon PLD activity was examined in human cancer cell lines where PLD activity provides a survival signal. The dependence of PLD survival signals on Ras was investigated, as was the effect of honokiol on Ras activation.

resultsWe report here that honokiol suppresses PLD activity in human cancer cells where PLD has been shown to suppress apoptosis. PLD activity is commonly elevated in response to the stress of serum withdrawal, and, importantly, the stress-induced increase in PLD activity is selectively suppressed by honokiol. The stress-induced increase in PLD activity was accompanied by increased Ras activation, and the stress-induced increase in PLD activity in MDA-MB-231 breast cancer cells was dependent on a Ras. The PLD activity was also dependent on the GTPases RalA and ADP ribosylation factor. Importantly, honokiol suppressed Ras activation.

conclusionThe data provided here indicate that honokiol may be a valuable therapeutic reagent for targeting a large number of human cancers that depend on Ras and PLD for their survival.

Indexed as

Allyl CompoundsAnimalsAntineoplastic Agents, PhytogenicApoptosisBiphenyl CompoundsCell Line, TumorCell SurvivalEnzyme ActivationHumansLignansMiceModels, ChemicalNeoplasmsNeoplasm TransplantationPhenolsPhospholipase DAllyl CompoundsAntineoplastic Agents, PhytogenicBiphenyl CompoundshonokiolLignansPhenolsPhospholipase Dras Proteins

Identifiers

PMID18594009
PMCPMC2759181
OpenAlexW2157529751

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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.