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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06409416
Other study ID # RF-2021-12372433
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 1, 2024
Est. completion date June 1, 2026

Study information

Verified date June 2024
Source Casa Sollievo della Sofferenza IRCCS
Contact Fabrizio Bianchi, PhD
Phone +390882416571
Email f.bianchi@operapadrepio.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Tumor cell plasticity (TCP) is a conubium of processes which lead to re-activation of developmental programs correlating with epithelial-to-mesenchymal transition, and ultimately leading to acquisition of stem cell properties and transdifferentiation potential. Little is known about the molecular mechanisms governing TCP in lung adenocarcinoma (LUAD), i.e. the most frequent lung cancer subtype. The investigators recently identified prognostic 7-miRNAs/10-mRNAs signatures which accurately identified aggressive LUAD among patients with early-stage disease (Stage I). Furthermore, the investigators showed that such tumors show TCP features i.e. mesenchymal and stem-cell traits, high-metastatic potential. Here, the investigators aim to explore by RNAseq and by immunophenotyping at a single-cell level (scRNAseq/AbSeq), the molecular features of aggressive LUAD to unveil the mechanisms triggering TCP. The investigators predict thier results will be relevant for the development of more effective therapeutic protocols for management of aggressive LUAD.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date June 1, 2026
Est. primary completion date June 1, 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - patients diagnosed with lung adenocarcinoma - treatment naive - undergoing primary surgery Exclusion Criteria: - patients with a previous history of cancer - previously treated by chemio/immuno/radio-therapy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Analysis of diagnostic biomarkers
The investigators will analyze TCP-biomarkers diagnostic by IHC, qRT-PCR and next-generation sequencing, in tumor and plasma samples of lung cancer patients.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Casa Sollievo della Sofferenza IRCCS IRCCS Ospedale San Raffaele

Outcome

Type Measure Description Time frame Safety issue
Primary TCP-biomarkers screening in a prospective cohort of lung cancer patients The investigators will: i) deconvolute the tumor epithelial cell heterogeneity of lung adenocarcinoma (LUAD) by coupling immunophenotype screening and single-cell RNAseq profiling of human LUAD samples; ii) identify subsets of LUAD cells with "active" tumor cell plasticity (TCP) using both our miRNA/RNA prognostic signatures, the C1-LUAD geneset (N=330), and previously identified signatures of lung cells high-cell plasticity (HCP) state; iii) explore the molecular features of TCP cell subsets by gene-network rewiring, pathway reconstruction analysis, and functional validation experiments of molecular "HUBs" controlling TCP pathways. Biomarkers of TCP will be also prioritized among TCP-hallmark genes and validated by immunohistochemistry (IHC/FACS) in human LUAD. 36 months
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