Shh Signaling in Brain AVMs: Novel Player & Therapeutic Target (SHAM)
Sonic Hedgehog Signaling: Novel Player and Potential Therapeutic Target in Brain Arteriovenous Malformations
The present study, entitled "SHAM Study," is a prospective observational translational study aimed at investigating the molecular mechanisms underlying brain arteriovenous malformations (AVMs). In particular, the study seeks to explore the role of the Sonic Hedgehog (Shh) signaling pathway, which has recently been hypothesized as a potential key player in pathological angiogenesis and in the maintenance of the malformative nidus.
The study will be conducted through the analysis of brain tissues obtained exclusively as residual material from neurosurgical procedures performed for clinical indications. Under no circumstances will additional procedures be carried out or modifications made to the patients' therapeutic pathway for research purposes. Samples will include tissues from adult patients undergoing AVM resection and, as controls, non-pathological brain tissues derived from surgeries performed for other indications, such as drug-resistant epilepsy.
The methodological approach involves the isolation of endothelial cells from collected samples and their characterization using multi-omics techniques, including transcriptomic analysis, microRNA profiling, and quantitative proteomics. The resulting data will be integrated through advanced bioinformatics analyses in order to identify specific molecular patterns, altered pathways, and potential biomarkers. Particular attention will be given to the evaluation of Shh pathway activation and its interactions with other signaling systems involved in AVM pathogenesis.
The collected biological material may also be used, subject to specific informed consent, for preclinical studies conducted on animal models, with the aim of further investigating the identified pathogenetic mechanisms and assessing their functional relevance. Such activities will be carried out in compliance with current regulations on animal experimentation and subject to approval by the relevant authorities.
The primary objective of the study is to identify significant differences in gene expression between endothelial cells derived from AVMs and control brain tissue. Secondary objectives include the identification of integrated molecular profiles (RNA, microRNA, and proteins), the correlation of these profiles with patients' clinical and radiological characteristics, and the identification of potential therapeutic targets.
The study is designed so as not to entail additional risks for participants, as it is based exclusively on the use of biological material that would otherwise be discarded. All subjects will be enrolled only after providing written informed consent. Data will be processed in pseudonymized form in compliance with current regulations on personal data protection.
The total expected duration is 36 months, and the study is part of a targeted research project aimed at generating new knowledge with potential translational impact, laying the groundwork for the future development of targeted therapeutic strategies.
Study duration and number of patients:
The overall duration of the study will be 36 months. Enrollment will begin immediately after ethical approval and will be completed by month 24.
A total of 30-45 adult patients are expected to be enrolled, including 20-30 undergoing resection of brain arteriovenous malformations and 10-15 patients undergoing neurosurgical procedures for drug-resistant epilepsy, from whom non-pathological cortical tissue will be obtained.
調査の概要
状態
研究の種類
入学 (推定)
連絡先と場所
研究場所
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Rome
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Rome、Rome、イタリア、00168
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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コンタクト:
- Roberto Pola, Professor, MD
- 電話番号:+39 0630151
- メール:roberto.pola@policlinicogemelli.it
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Adult patients aged 18 years or older undergoing neurosurgical resection who provide written informed consent for research use of residual tissue.
Exclusion Criteria:
- Tissue with extensive necrosis or contamination, lack of valid consent, or known infectious agents that preclude safe handling.
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
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AVM group (cases)
Adult patients undergoing neurosurgical resection of brain arteriovenous malformations for clinically indicated reasons.
Residual AVM tissue obtained during surgery will be used for molecular analyses.
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Control group
Adult patients undergoing neurosurgical procedures for drug-resistant epilepsy or other clinical indications, from whom non-pathological brain tissue is resected as part of standard care.
Residual tissue will be used as control.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Differential endothelial gene expression between AVM and control tissues.
時間枠:Up to 34 months
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Endothelial differential gene expression measured as log2 fold change and adjusted p value from bulk RNA seq.
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Up to 34 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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MicroRNA and proteomic profiles, pathway activity scores, histological markers, and clinical correlations.
時間枠:Up to 34 months
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MicroRNA abundance (normalized counts); protein abundance (LFQ intensity); pathway activity scores (Shh, Notch, VEGF, TGF β/ALK1, MAPK); histological metrics (percent positive area; mean staining intensity for Shh, Gli1, CD31, α SMA).
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Up to 34 months
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
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Single-cell analyses, integrated biomarkers, and potential therapeutic targets.
時間枠:Up to 36 months
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Identification of single-cell transcriptional clusters and inferred cell-type composition, where single-cell data are available. Identification of integrated multi-omics biomarker panels based on concordant transcriptomic and proteomic signals. Identification of candidate druggable targets prioritized through network centrality analyses and cross-platform validation. |
Up to 36 months
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協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- 27587
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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