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Netrin-1 & Hepatocellular Carcinoma HCC

Netrin-1 in Hepatocellular Carcinoma: Pathology, Preclinical Targeting, and Definition of Eligibility Criteria for Phase 1 Trials

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04766736
Acronym
HCC-Net
Enrollment
320
Registered
2021-02-23
Start date
2019-07-01
Completion date
2022-12-31
Last updated
2021-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCC

Brief summary

Netrin-1 is a dependence receptor ligand participating in the pathology of several cancer types. It is up-regulated in chronic liver diseases, cirrhosis and HCC. We hypothesize that netrin-1 may play a detrimental role in HCC. The goal of this project is to characterize netrin-1 signals in HCC samples with ad hoc controls, to investigate the benefit of capturing netrin-1 in preclinical models of HCC and to try to define patients groups the most likely to benefit from this targeting approach in the clinic.

Interventions

PROCEDUREQuantification of netrin-1 signals by antibody-based approaches

Samples have been obtained upon curative surgery without any other therapy administered and subsequently characterized by pathologists after FFPE inclusion.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* any patient suffering from HCC * age \>18 * informed consent provided

Exclusion criteria

\- absence of informed consent

Design outcomes

Primary

MeasureTime frameDescription
Netrin-1 expression patterns in HCC samplesOutcome measure is to be performed after surgery of the tumors (at least 1 year later). It has no impact on the patient's care.Netrin-1 expression levels will be quantified by immunoblotting with ad hoc internal standards. Positivity threshold by IHC will be evaluated using ad hoc positive and negative control tissues. The densitometry approach will be used.

Countries

France

Contacts

Primary ContactFabien ZOULIM, Pr
fabien.zoulim@chu-lyon.fr4 26 10 93 55
Backup ContactRomain PARENT
romain.parent@inserm.fr4 72 68 19 70

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026