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Ramezani, S.

Publications and source records attributed to Ramezani, S..

3 recordsLinked to original sources

Antibody-Protein L Functionalized Microparticles for Detection of Surface Markers in Heterogeneous Colorectal Lesions

Visualization of colorectal cancer (CRC) lesions is complicated by their location in the colon and tumor morphology. Reliance on a single surface biomarker for direct identification risks false negatives due to temporal changes and/or tumor heterogeneity. We developed a multiplexed system of complementary biomarker targets in an effort to capture a broader range of lesions with diverse temporal and/or phenotypic expression. We identified Mucin-1 (MUC1) and epithelial cell adhesion molecule (EPCAM) as useful targeting pairs by examining multiple colon tumor subtypes in a standard tissue array, and by surveying multiple CRC cell lines, both as 2D cultures and as 3D tumoroids, for the presence of the CRC surface biomarkers. We demonstrated the utility of a "universal" surface functionalization approach using Antibody-Protein L functionalized microparticles (APL-MPs) that enabled the simultaneous incorporation of antibodies recognizing MUC1 and EPCAM. Using CRC cell heterogeneous tumoroids expressing both MUC1 and EPCAM (HET-tumoroids) and orthotopic animal cancer models designed to express both surface antigens, we demonstrated that: 1) APL-MPs identified MUC1- and EPCAM-positive tumoroids in proportion to antigen expression; 2) APL-MPs detected CRC surface antigens on the luminal colon surface in vivo, and 3) concurrent targeting of multiple surface antigens enhanced the sensitivity of detection of heterogeneous CRC lesions. This approach opens the door for the use of antibody-protein L dual-targeting MPs in a variety of applications to detect heterogeneous cancer lesions. SignificanceMulti-antigen targeting of MUC1 and EPCAM with Antibody-Protein L microparticles enhances the detection sensitivity of heterogeneous colorectal cancer lesions, offering a promising strategy for the accurate visualization of tumors in complex environments.

cancer biology↗

Inhibitory Properties of Cannabis sativa Seed Extract on Pancreatic Cancer Cells

BackgroundPancreatic Ductal Adenocarcinoma (PDAC) is one of the most lethal cancers and there is a pressing need for development of new therapies. Recently, cannabis has received attentions as a promising plant-based medication for treating a variety of illnesses. The studies investigating the anti-tumor effects of C. sativa extract, to date, have used the plant leaves. In this study, we explore the inhibitory properties of C. sativa seeds. MethodsAn ethanolic extract of C. sativa seeds was prepared. GC-MS analysis was performed to identify the compounds in the extract. The cytotoxicity of the extract on PANC-1 cells and HFF cells was assessed using MTT assay. Colony formation and Wound healing assays were used to evaluate the impact of the extract on the ability of PANC-1 cells to form colonies and migrate. Flow cytometry analysis evaluated cell cycle phase of PANC-1 cells after treatment with the extract. ResultsThe C. sativa seed extract had anti-proliferative effects on pancreatic cancer cells PANC-1, while showing no such an effect on normal HFF cells. The extract made its impact on PANC-1 cells by arresting them at G1 phase and increasing their apoptosis. Furthermore it inhibited PANC-1 colony formation and changed the colony combination in favor of paraclones. Migration capacity of PANC-1 cells was also attenuated by the extract. ConclusionsOur results revealed that C. sativa seed extract has inhibitory effects on PANC-1 cells by reducing their proliferation, migration and colony formation capacity. It halts the cells in G1 phase and increases their apoptosis.

cancer biology↗

Targeted Molecular MRI of Colorectal Cancer by Antibody Functionalized Hyperpolarized Silicon Particles

The development of non-invasive, non-ionizing sensitive molecular targeting approaches to detect colorectal cancer (CRC) lesions is warranted to improve high risk patient outcomes. Hyperpolarized silicon nanoparticles and microparticles are potentially well-suited to act as targeted molecular imaging agents because of their overall biocompatibility and long-lasting enhanced magnetic resonance imaging (MRI) signals. In this study, dynamic nuclear polarization was performed on silicon particles functionalized with an antibody to Mucin-1 (MUC1), a surface mucin glycoprotein aberrantly expressed in CRC. Antibody conjugation to the particle surface did not affect 29Si hyperpolarization characteristics. Similarly, conjugation and the dynamic nuclear polarization process did not adversely affect the affinity of the targeting antibody. In vivo MRI scans performed 10-15 minutes after luminal administration of targeted hyperpolarized particles into human MUC1-expressing orthotopic CRC mouse models showed that particles actively targeted tumor sites. These results were supported by chemical and biological controls and blocking experiments as well as correlative immunohistochemical analysis. These surface-functionalized silicon particles are under development as a platform technology that will allow non-invasive molecular targeting of CRC using hyperpolarized MRI. Single Sentence SummaryTargeted molecular MR imaging of colorectal cancer by hyperpolarized silicon particles functionalized with mucin 1 antibody.

cancer biology↗