Evidence map›Paper›PMID 18758481›Full record

ReviewOncogene2008

Rational targeting of Notch signaling in cancer.

P Rizzo, C Osipo, K Foreman, T Golde, B Osborne, L Miele

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 224 papers.

0numbers the graph read from it
0cells of the map it votes in
224citing papers in PubMed
16.3field-weighted citation impact, top 1% 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

224 citing papers in PubMed, 411 citations in OpenAlex.

  1. A phase II study of RO4929097 in metastatic colorectal cancer.European journal of cancer (Oxford, England : 1990) · 2012
    Trial
  2. The miRNA-4330/ABCG2 axis overcomes drug resistance and cancer progression in both ER-positive and ER-negative resistant breast cancer cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  3. The Role ofCancers · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. The Intricate Notch Signaling Dynamics in Therapeutic Realms of Cancer.ACS pharmacology & translational science · 2023
    Review
  17. Notch Signaling in Acute Inflammation and Sepsis.International journal of molecular sciences · 2023
    Review
  18. Article
  19. International journal of molecular sciences · 2023
    Article
  20. Review

164 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

P RizzoBreast Cancer Program, Cardinal Bernardin Cancer Center, Loyola University Chicago, Chicago, IL 60163, USA.
C Osipo
K Foreman
T Golde
B Osborne
L Miele
Loyola University Chicago · USMayo Clinic · US

Funding

Targeting Multiple Diseases Through Gamma SecretaseP01AG025531 · NIA · UNIVERSITY OF MASSACHUSETTS AMHERST · PI OSBORNE, BARBARA A · 2006 to 2011
$5.0M
NIA NIH HHS P01 AG2553101
6 · The paper itself

Abstract

Accumulating preclinical and clinical evidence supports a pro-oncogenic function for Notch signaling in several solid tumors, particularly but not exclusively in breast cancer. Notch inhibitory agents, such as gamma-secretase inhibitors, are being investigated as candidate cancer therapeutic agents. Interest in therapeutic modulation of the Notch pathway has been increased by recent reports, indicating that its role is important in controlling the fate of putative 'breast cancer stem cells'. However, as is the case for most targeted therapies, successful targeting of Notch signaling in cancer will require a considerable refinement of our understanding of the regulation of this pathway and its effects in both normal and cancer cells. Notch signaling has bidirectional 'cross talk' interaction with multiple other pathways that include candidate therapeutic targets. Understanding these interactions will greatly increase our ability to design rational combination regimens. To determine which patients are most likely to benefit from treatment with Notch inhibitors, it will be necessary to develop molecular tests to accurately measure pathway activity in specific tumors. Finally, mechanism-based toxicities will have to be addressed by a careful choice of therapeutic agents, combinations and regimens. This article summarizes the current state of the field, and briefly describes opportunities and challenges for Notch-targeted therapies in oncology.

Indexed as

Amyloid Precursor Protein SecretasesAntibodies, MonoclonalAntineoplastic AgentsApoptosisBiological ProductsCell DivisionCombined Modality TherapyDrug Delivery SystemsDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansNeoplasm ProteinsNeoplasmsNeoplastic Stem CellsPluripotent Stem CellsAmyloid Precursor Protein SecretasesAntibodies, MonoclonalAntineoplastic AgentsBiological ProductsNeoplasm ProteinsReceptors, NotchTumor Suppressor Proteins

Identifiers

PMID18758481
OpenAlexW2062069005

What OpenQuestion holds

Textmetadata
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.