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  1. AU="Caparello, Basilio"
  2. AU="Fricke, T T"
  3. AU="Mummery, C J"
  4. AU="Krantz, Emily"
  5. AU="Bedoya-Arias, Juan E"
  6. AU="Zhou, Heyang"
  7. AU=Latson Larry A
  8. AU=Alhuzimi Eman
  9. AU="Wuerzberger-Davis, Shelly M"
  10. AU="Clippinger, Amy J"
  11. AU="M. S. Islam"
  12. AU="Borrego-Jiménez, Jaime"
  13. AU="Kaoru Dohi"
  14. AU="Tornai, Gábor J"
  15. AU="D'Avella, Christopher"
  16. AU="Lim, Boon L."
  17. AU="Heselden, Marie"
  18. AU=Dias?Polak David
  19. AU="Shahid Umar"
  20. AU="Abu-Shmais, Alexandria A"
  21. AU="Takenaka, Haruka"
  22. AU="Bramley, Andrea"
  23. AU="Sang Hong Lee"

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  1. Artikel ; Online: TERRA G-quadruplex stabilization as a new therapeutic strategy for multiple myeloma.

    Scionti, Francesca / Juli, Giada / Rocca, Roberta / Polerà, Nicoletta / Nadai, Matteo / Grillone, Katia / Caracciolo, Daniele / Riillo, Caterina / Altomare, Emanuela / Ascrizzi, Serena / Caparello, Basilio / Cerra, Maria / Arbitrio, Mariamena / Richter, Sara N / Artese, Anna / Alcaro, Stefano / Tagliaferri, Pierosandro / Tassone, Pierfrancesco / Di Martino, Maria Teresa

    Journal of experimental & clinical cancer research : CR

    2023  Band 42, Heft 1, Seite(n) 71

    Abstract: Background: Multiple myeloma (MM) is a hematologic malignancy characterized by high genomic instability, and telomere dysfunction is an important cause of acquired genomic alterations. Telomeric repeat-containing RNA (TERRA) transcripts are long non- ... ...

    Abstract Background: Multiple myeloma (MM) is a hematologic malignancy characterized by high genomic instability, and telomere dysfunction is an important cause of acquired genomic alterations. Telomeric repeat-containing RNA (TERRA) transcripts are long non-coding RNAs involved in telomere stability through the interaction with shelterin complex. Dysregulation of TERRAs has been reported across several cancer types. We recently identified a small molecule, hit 17, which stabilizes the secondary structure of TERRA. In this study, we investigated in vitro and in vivo anti-MM activities of hit 17.
    Methods: Anti-proliferative activity of hit 17 was evaluated in different MM cell lines by cell proliferation assay, and the apoptotic process was analyzed by flow cytometry. Gene and protein expressions were detected by RT-qPCR and western blotting, respectively. Microarray analysis was used to analyze the transcriptome profile. The effect of hit 17 on telomeric structure was evaluated by chromatin immunoprecipitation. Further evaluation in vivo was proceeded upon NCI-H929 and AMO-1 xenograft models.
    Results: TERRA G4 stabilization induced in vitro dissociation of telomeric repeat-binding factor 2 (TRF2) from telomeres leading to the activation of ATM-dependent DNA damage response, cell cycle arrest, proliferation block, and apoptotic death in MM cell lines. In addition, up-regulation of TERRA transcription was observed upon DNA damage and TRF2 loss. Transcriptome analysis followed by gene set enrichment analysis (GSEA) confirmed the involvement of the above-mentioned processes and other pathways such as E2F, MYC, oxidative phosphorylation, and DNA repair genes as early events following hit 17-induced TERRA stabilization. Moreover, hit 17 exerted anti-tumor activity against MM xenograft models.
    Conclusion: Our findings provide evidence that targeting TERRA by hit 17 could represent a promising strategy for a novel therapeutic approach to MM.
    Mesh-Begriff(e) Humans ; Multiple Myeloma/drug therapy ; Multiple Myeloma/genetics ; Telomere ; Transcription, Genetic ; Apoptosis ; Transcriptome
    Sprache Englisch
    Erscheinungsdatum 2023-03-27
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 803138-1
    ISSN 1756-9966 ; 0392-9078
    ISSN (online) 1756-9966
    ISSN 0392-9078
    DOI 10.1186/s13046-023-02633-0
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: A Pronectin™ AXL-targeted first-in-class bispecific T cell engager (pAXLxCD3ε) for ovarian cancer.

    Riillo, Caterina / Polerà, Nicoletta / Di Martino, Maria Teresa / Juli, Giada / Hokanson, Craig A / Odineca, Tatjana / Signorelli, Stefania / Grillone, Katia / Ascrizzi, Serena / Mancuso, Antonia / Staropoli, Nicoletta / Caparello, Basilio / Cerra, Maria / Nisticò, Giuseppe / Tagliaferri, Pierosandro / Crea, Roberto / Caracciolo, Daniele / Tassone, Pierfrancesco

    Journal of translational medicine

    2023  Band 21, Heft 1, Seite(n) 301

    Abstract: Background: Pronectins™ are a new class of fibronectin-3-domain 14th-derived (14Fn3) antibody mimics that can be engineered as bispecific T cell engager (BTCE) to redirect immune effector cells against cancer. We describe here the in vitro and in vivo ... ...

    Abstract Background: Pronectins™ are a new class of fibronectin-3-domain 14th-derived (14Fn3) antibody mimics that can be engineered as bispecific T cell engager (BTCE) to redirect immune effector cells against cancer. We describe here the in vitro and in vivo activity of a Pronectin™ AXL-targeted first-in-class bispecific T cell engager (pAXLxCD3ε) against Epithelial Ovarian Cancer (EOC).
    Methods: pAXLxCD3ε T-cell mediated cytotoxicity was evaluated by flow cytometry and bioluminescence. pAXLxCD3ε mediated T-cell infiltration, activation and proliferation were assessed by immunofluorescence microscopy and by flow cytometry. Activity of pAXLxCD3ε was also investigated in combination with poly-ADP ribose polymerase inhibitors (PARPi). In vivo antitumor activity of pAXLxCD3ε was evaluated in immunocompromised (NSG) mice bearing intraperitoneal or subcutaneous EOC xenografts and immunologically reconstituted with human peripheral blood mononuclear cells (PBMC).
    Results: pAXLxCD3ε induced dose-dependent cytotoxicity by activation of T lymphocytes against EOC cells, regardless of their histologic origin. The addition of PARPi to cell cultures enhanced pAXLxCD3ε cytotoxicity. Importantly, in vivo, pAXLxCD3ε was highly effective against EOC xenografts in two different NSG mouse models, by inhibiting the growth of tumor cells in ascites and subcutaneous xenografts. This effect translated into a significantly prolonged survival of treated animals.
    Conclusion: pAXLxCD3ε is an active therapeutics against EOC cells providing a rational for its development as a novel agent in this still incurable disease. The preclinical validation of a first-in-class agent opens the way to the development of a new 14Fn3-based scaffold platform for the generation of innovative immune therapeutics against cancer.
    Mesh-Begriff(e) Humans ; Mice ; Animals ; Female ; Leukocytes, Mononuclear ; Antibodies, Bispecific/pharmacology ; Antibodies, Bispecific/therapeutic use ; Ovarian Neoplasms/drug therapy ; T-Lymphocytes ; Carcinoma, Ovarian Epithelial ; Cell Line, Tumor ; CD3 Complex
    Chemische Substanzen Antibodies, Bispecific ; CD3 Complex
    Sprache Englisch
    Erscheinungsdatum 2023-05-04
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2118570-0
    ISSN 1479-5876 ; 1479-5876
    ISSN (online) 1479-5876
    ISSN 1479-5876
    DOI 10.1186/s12967-023-04101-x
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Exploiting DNA Ligase III addiction of multiple myeloma by flavonoid Rhamnetin.

    Caracciolo, Daniele / Juli, Giada / Riillo, Caterina / Coricello, Adriana / Vasile, Francesca / Pollastri, Sara / Rocca, Roberta / Scionti, Francesca / Polerà, Nicoletta / Grillone, Katia / Arbitrio, Mariamena / Staropoli, Nicoletta / Caparello, Basilio / Britti, Domenico / Loprete, Giovanni / Costa, Giosuè / Di Martino, Maria Teresa / Alcaro, Stefano / Tagliaferri, Pierosandro /
    Tassone, Pierfrancesco

    Journal of translational medicine

    2022  Band 20, Heft 1, Seite(n) 482

    Abstract: Background: DNA ligases are crucial for DNA repair and cell replication since they catalyze the final steps in which DNA breaks are joined. DNA Ligase III (LIG3) exerts a pivotal role in Alternative-Non-Homologous End Joining Repair (Alt-NHEJ), an error- ...

    Abstract Background: DNA ligases are crucial for DNA repair and cell replication since they catalyze the final steps in which DNA breaks are joined. DNA Ligase III (LIG3) exerts a pivotal role in Alternative-Non-Homologous End Joining Repair (Alt-NHEJ), an error-prone DNA repair pathway often up-regulated in genomically unstable cancer, such as Multiple Myeloma (MM). Based on the three-dimensional (3D) LIG3 structure, we performed a computational screening to identify LIG3-targeting natural compounds as potential candidates to counteract Alt-NHEJ activity in MM.
    Methods: Virtual screening was conducted by interrogating the Phenol Explorer database. Validation of binding to LIG3 recombinant protein was performed by Saturation Transfer Difference (STD)-nuclear magnetic resonance (NMR) experiments. Cell viability was analyzed by Cell Titer-Glo assay; apoptosis was evaluated by flow cytometric analysis following Annexin V-7AAD staining. Alt-NHEJ repair modulation was evaluated using plasmid re-joining assay and Cytoscan HD. DNA Damage Response protein levels were analyzed by Western blot of whole and fractionated protein extracts and immunofluorescence analysis. The mitochondrial DNA (mtDNA) copy number was determined by qPCR. In vivo activity was evaluated in NOD-SCID mice subcutaneously engrafted with MM cells.
    Results: Here, we provide evidence that a natural flavonoid Rhamnetin (RHM), selected by a computational approach, counteracts LIG3 activity and killed Alt-NHEJ-dependent MM cells. Indeed, Nuclear Magnetic Resonance (NMR) showed binding of RHM to LIG3 protein and functional experiments revealed that RHM interferes with LIG3-driven nuclear and mitochondrial DNA repair, leading to significant anti-MM activity in vitro and in vivo.
    Conclusion: Taken together, our findings provide proof of concept that RHM targets LIG3 addiction in MM and may represent therefore a novel promising anti-tumor natural agent to be investigated in an early clinical setting.
    Mesh-Begriff(e) Animals ; Mice ; Annexin A5/genetics ; Annexin A5/metabolism ; DNA Ligase ATP/genetics ; DNA Ligase ATP/metabolism ; DNA Ligases/chemistry ; DNA Ligases/genetics ; DNA Ligases/metabolism ; DNA Repair/drug effects ; DNA Repair/genetics ; DNA, Mitochondrial/drug effects ; DNA, Mitochondrial/genetics ; DNA, Mitochondrial/metabolism ; Flavonoids/pharmacology ; Flavonoids/therapeutic use ; Mice, Inbred NOD ; Mice, SCID ; Multiple Myeloma/drug therapy ; Multiple Myeloma/genetics ; Multiple Myeloma/metabolism ; Phenols ; Recombinant Proteins/metabolism
    Chemische Substanzen Annexin A5 ; DNA Ligase ATP (EC 6.5.1.1) ; DNA Ligases (EC 6.5.1.-) ; DNA, Mitochondrial ; Flavonoids ; Phenols ; Recombinant Proteins ; rhamnetin (71803L5F4S)
    Sprache Englisch
    Erscheinungsdatum 2022-10-22
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2118570-0
    ISSN 1479-5876 ; 1479-5876
    ISSN (online) 1479-5876
    ISSN 1479-5876
    DOI 10.1186/s12967-022-03705-z
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Age dependent switching role of cyclin D1 in breast cancer.

    Rinaldi, Carmela / Malara, Natalia Maria / D'Angelo, Rosalia / Sidoti, Antonina / Leotta, Attilio / Lio, Santo / Caparello, Basilio / Ruggeri, Alessia / Mollace, Vincenzo / Amato, Aldo

    Analytical cellular pathology (Amsterdam)

    2012  Band 35, Heft 3, Seite(n) 179–185

    Abstract: Background: Cyclin D1 gene (CCND1) plays pivotal roles in the development of several human cancers, including breast cancer, functioning as an oncogene. The aim of this study was to better understand the molecular dynamics of ductal carcinomas with ... ...

    Abstract Background: Cyclin D1 gene (CCND1) plays pivotal roles in the development of several human cancers, including breast cancer, functioning as an oncogene. The aim of this study was to better understand the molecular dynamics of ductal carcinomas with regard to proliferation and the ageing process.
    Methods: 130 cases of ductal breast cancer in postmenopausal women, aged 52-96 in 3 age classes were selected. Tumoral tissues preserved in formaldehyde solution and subsequently embedded in paraffin were subjected to analysis Fluorescence in situ Hybridization (FISH), Reverse Transcription-Polymerase Chain Reaction (RT- PCR) and immuno-histochemical tests. The molecular variables studied were estimated in relation to the patients' age.
    Results: The results obtained suggest that the increment of the levels of cyclin D1 in intra-ductal breast tumors in older woman that we have examined is significantly associated with a lower proliferation rate.
    Conclusion: Cyclin D1, which characterizes tumor in young women as molecular director involved in strengthening tumoral proliferation mechanisms, may be seen as a potential blocking molecular switch in corresponding tumours in old women.
    Mesh-Begriff(e) Aged ; Aged, 80 and over ; Aging/genetics ; Aging/physiology ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Breast Neoplasms/genetics ; Breast Neoplasms/metabolism ; Breast Neoplasms/physiopathology ; Cell Cycle/genetics ; Cell Cycle Proteins/genetics ; Cell Cycle Proteins/physiology ; Cell Proliferation ; Cell Transformation, Neoplastic/genetics ; Cell Transformation, Neoplastic/pathology ; Cyclin D1/genetics ; Cyclin D1/physiology ; Female ; Genes, Tumor Suppressor/physiology ; Humans ; Middle Aged ; Up-Regulation/genetics
    Chemische Substanzen Biomarkers, Tumor ; CCND1 protein, human ; Cell Cycle Proteins ; Cyclin D1 (136601-57-5)
    Sprache Englisch
    Erscheinungsdatum 2012-01-09
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2583629-8
    ISSN 2210-7185 ; 2210-7177
    ISSN (online) 2210-7185
    ISSN 2210-7177
    DOI 10.3233/ACP-2011-0052
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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