Anticancer Activity of Novel Difluorinated Curcumin Analog and Its Inclusion Complex with 2-Hydroxypropyl-β-Cyclodextrin against Pancreatic Cancer DOI Open Access

Sangita Bhattacharyya,

Hindole Ghosh,

Obdulia Covarrubias‐Zambrano

et al.

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(7), P. 6336 - 6336

Published: March 28, 2023

Pancreatic ductal adenocarcinoma (PDAC) is the primary reason for cancer-related deaths in US. Genetic mutations, drug resistance, involvement of multiple signaling pathways, cancer stem cells (CSCs), and desmoplastic stroma, which hinders penetrance, contribute to poor chemotherapeutic efficacy. Hence, there a need identify novel drugs with improved delivery improve treatment outcomes. Curcumin one such compound that can inhibit pathways CSCs. However, curcumin’s clinical applicability treating PDAC limited because its solubility water metabolic instability. we developed difluorinated curcumin (CDF) analog accumulates selectively pancreas inhibits growth vitro vivo. In present work, 2-hydroxy-propyl-β-cyclodextrin (HCD) inclusion complex increase hydrolytic stability. The CDFHCD was characterized by spectroscopic, thermal, microscopic techniques. exhibited increased aqueous solubility, stability, antiproliferative activity compared parent CDF. Moreover, CDF inhibited colony spheroid formation, induced cell cycle apoptosis lines. self-assembly an efficient approach anticancer therapeutic efficacy, now warrants advancement towards proof concept patients.

Language: Английский

Ferroptosis- and stemness inhibition-mediated therapeutic potency of ferrous oxide nanoparticles-diethyldithiocarbamate using a co-spheroid 3D model of pancreatic cancer DOI Creative Commons
Marwa M. Abu‐Serie, Ana K. Gutiérrez-García,

Macie Enman

et al.

Journal of Gastroenterology, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 31, 2025

Language: Английский

Citations

0

Endocytosis: the match point of nanoparticle-based cancer therapy DOI
Yonglu Li, Xin Gao, Yapeng Li

et al.

Journal of Materials Chemistry B, Journal Year: 2024, Volume and Issue: 12(38), P. 9435 - 9458

Published: Jan. 1, 2024

Nanomedicine has inspired a ground-breaking strategy for cancer therapy. By intelligently assembling diverse moieties to form nanoparticles, numerous functionalities such as controlled release, synergistic efficiency, and

Language: Английский

Citations

3

Functional Characterization of miR-216a-5p and miR-125a-5p on Pancreatic Cancer Stem Cells DOI Open Access
Grazia Fenu, Carmen Griñán‐Lisón, Federica Etzi

et al.

International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(7), P. 2830 - 2830

Published: March 21, 2025

Pancreatic ductal adenocarcinoma (PDAC) is the third leading cause of cancer-related death. Its poor prognosis closely related to late-stage diagnosis, which results from both nonspecific symptoms and absence biomarkers for early diagnosis. MicroRNAs (miRNAs) exert a regulatory role in numerous biological processes their aberrant expression has been found broad spectrum diseases, including cancer. Cancer stem cells (CSCs) represent driving force PDAC initiation, progression, metastatic spread. Our previous research highlighted interesting behavior miR-216a-5p miR-125a-5p progression CSC phenotype. The present study aimed evaluate effect on acquisition or suppression pancreatic traits. BxPC-3, AsPC-1 cell lines, CSC-like models were transfected with mimics inhibitors. Following transfection, we evaluated impact surface markers (CD44/CD24/CxCR4), ALDH1 activity, pluripotency- EMT-related gene expression, clonogenic potential. show that enhances CD44/CD24/CxCR4 while negatively affecting activity EMT genes. MiR-216a-5p positively influenced property. MiR-125a-5p promoted inhibiting activity. It enhanced Snail, Oct-4, Sox-2, potential appeared be affected. Comprehensively, our provide further knowledge miRNAs CSCs. Moreover, they corroborate findings about miR-216a-5p’s dual miR-125a-5p’s promotive function PDAC.

Language: Английский

Citations

0

Multifaceted Pharmacological Potentials of Curcumin, Genistein, and Tanshinone IIA through Proteomic Approaches: An In-Depth Review DOI Open Access
Mir Azam Khan, Parul Singh, Yahya F. Jamous

et al.

Cancers, Journal Year: 2022, Volume and Issue: 15(1), P. 249 - 249

Published: Dec. 30, 2022

Phytochemicals possess various intriguing pharmacological properties against diverse pathological conditions. Extensive studies are on-going to understand the structural/functional of phytochemicals as well molecular mechanisms their therapeutic function disease such curcumin (Cur), genistein (Gen), and tanshinone-IIA (Tan IIA) have multifaceted potentials efforts in progress dynamics with different tools technologies. Cur is an active lipophilic polyphenol pleiotropic function, it has been shown including antioxidant, anti-inflammatory, anti-microbial, anticancer, anti-genotoxic besides others beneficial properties. Similarly, Gen (an isoflavone) exhibits a wide range vital functions pro-apoptotic, anti-proliferative, anti-angiogenic activities etc. In addition, Tan IIA, compound, possesses anti-angiogenic, anticancer activities, so on. Over last few decades, field proteomics garnered great momentum mainly attributed recent advancement mass spectrometry (MS) techniques. It envisaged that technology considerably contributed biomedical research endeavors lately. Interestingly, they also explored reliable approach intricacies related phytochemical-based interventions. The present review provides overview performed unravel underlying Cur, Gen, IIA. This in-depth study will help researchers better understanding potential at level. Certainly, this be highly instrumental catalyzing translational shift from clinical practice near future.

Language: Английский

Citations

15

Anticancer Activity of Novel Difluorinated Curcumin Analog and Its Inclusion Complex with 2-Hydroxypropyl-β-Cyclodextrin against Pancreatic Cancer DOI Open Access

Sangita Bhattacharyya,

Hindole Ghosh,

Obdulia Covarrubias‐Zambrano

et al.

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(7), P. 6336 - 6336

Published: March 28, 2023

Pancreatic ductal adenocarcinoma (PDAC) is the primary reason for cancer-related deaths in US. Genetic mutations, drug resistance, involvement of multiple signaling pathways, cancer stem cells (CSCs), and desmoplastic stroma, which hinders penetrance, contribute to poor chemotherapeutic efficacy. Hence, there a need identify novel drugs with improved delivery improve treatment outcomes. Curcumin one such compound that can inhibit pathways CSCs. However, curcumin’s clinical applicability treating PDAC limited because its solubility water metabolic instability. we developed difluorinated curcumin (CDF) analog accumulates selectively pancreas inhibits growth vitro vivo. In present work, 2-hydroxy-propyl-β-cyclodextrin (HCD) inclusion complex increase hydrolytic stability. The CDFHCD was characterized by spectroscopic, thermal, microscopic techniques. exhibited increased aqueous solubility, stability, antiproliferative activity compared parent CDF. Moreover, CDF inhibited colony spheroid formation, induced cell cycle apoptosis lines. self-assembly an efficient approach anticancer therapeutic efficacy, now warrants advancement towards proof concept patients.

Language: Английский

Citations

8