Sabina Quader

Dr. Sabina Quader

Innovation Center of NanoMedicine, Kawasaki Institute of Industrial Promotion, Kawasaki, Japan
orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 June 2020 in Frontiers in Pharmacology
Verified
Journal Article
Open access
PDF file
Shihori TanabeShihori Tanabe
Shihori Tanabe
Sabina QuaderSabina Quader
Sabina Quader
HCHoracio Cabral
Horacio Cabral
RORyuichi Ono
Ryuichi Ono
The mechanism of epithelial-mesenchymal transition (EMT) consists of the cellular phenotypic transition from epithelial to mesenchymal status. The cells exhibiting EMT exist in cancer stem cell (CSC) population, which is involved in drug resistance. CSCs demonstrating EMT feature remain after cancer treatment, which leads to drug resistance, recurrence, metastasis and malignancy of cancer. In this context, the recent advance of nanotechnology in the medical application has ascended the possibility to target CSCs using nanomedicines. In this review article, we focused on the mechanism of CSCs and EMT, especially into the signaling pathways in EMT, regulation of EMT and CSCs by microRNAs and nanomedicine-based approaches to target CSCs.

1 July 2017 in Molecular Therapy
Verified
Journal Article
Open access
Sabina QuaderSabina Quader
Sabina Quader
Kazunori KataokaKazunori Kataoka
Kazunori Kataoka
While cancer remains the major cause of death worldwide, nanomaterial (NM)-based diagnosis and treatment modalities are showing remarkable potential to better tackle clinical oncology by effectively targeting therapeutic agents to tumors. NMs can selectively accumulate in solid tumors, and they can improve the bioavailability and reduce the toxicity of encapsulated cytotoxic agents. Additional noteworthy functions of NMs in cancer treatment include the delivery of contrast agents to image tumor sites, delivery of genetic materials for gene therapy, and co-delivery of multiple agents to achieve combination therapy or simultaneous diagnostic and therapeutic outcomes. Although several NM therapeutics have been successfully translated to clinical applications, the gap between the bench and the bedside remains ominously wide. Tumor heterogeneity and the disparity between pre-clinical and clinical studies have been identified as two of the major translational challenges of NM-based cancer therapies. Herein, we review a handful of recent research studies on the use of NMs in cancer therapy and imaging, with a limited discussion on the consequences of tumor heterogeneity and pre-clinical studies on translational research of NM-based delivery systems and propositions in the literature to overcome these challenges.

22 January 2022 in Advanced Drug Delivery Reviews
Verified
Journal Article
Closed access
Sabina QuaderSabina Quader
Sabina Quader
Kazunori KataokaKazunori Kataoka
Kazunori Kataoka
Horacio CabralHoracio Cabral
Horacio Cabral

1 July 2017 in Journal of Controlled Release
Verified
Journal Article
Closed access
Sabina QuaderSabina Quader
Sabina Quader
XLX. Liu
X. Liu
Yi-Chun ChenYi-Chun Chen
Yi-Chun Chen
PMP. Mi
P. Mi
TCT. Chida
T. Chida
Kazunori KataokaKazunori Kataoka
Kazunori Kataoka

12 June 2019 in ACS Nano
Verified
Journal Article
Closed access
JMJohn D. Martin
John D. Martin
MPMyrofora Panagi
Myrofora Panagi
CWChenyu Wang
Chenyu Wang
TKThahomina T. Khan
Thahomina T. Khan
MMMargaret R. Martin
Margaret R. Martin
Horacio CabralHoracio Cabral
Horacio Cabral

20 May 2020 in ACS Nano
Verified
Journal Article
Closed access
JXJinbing Xie
Jinbing Xie
DCDaniel Gonzalez Carter
Daniel Gonzalez Carter
TTTheofilus A. Tockary
Theofilus A. Tockary
NNNoriko Nakamura
Noriko Nakamura
YXYonger Xue
Yonger Xue
Kazunori KataokaKazunori Kataoka
Kazunori Kataoka