Hafize Aysin Akpinar

ORCID: 0000-0002-6718-6343
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About
Contact & Profiles
Research Areas
  • Autophagy in Disease and Therapy
  • Ubiquitin and proteasome pathways
  • CAR-T cell therapy research
  • Cannabis and Cannabinoid Research
  • bioluminescence and chemiluminescence research
  • Lymphoma Diagnosis and Treatment
  • Lipid metabolism and biosynthesis
  • Protein Degradation and Inhibitors
  • Mycotoxins in Agriculture and Food
  • Crystallization and Solubility Studies
  • Parkinson's Disease Mechanisms and Treatments
  • Cancer therapeutics and mechanisms
  • X-ray Diffraction in Crystallography

Institute of Cancer Research
2019-2023

Cancer Research UK
2019-2022

Boğaziçi University
2019

Daniel J. Klionsky Amal Kamal Abdel‐Aziz Sara Abdelfatah Mahmoud Abdellatif Asghar Abdoli and 95 more Steffen Abel Hagai Abeliovich Marie H. Abildgaard Yakubu Princely Abudu Abraham Acevedo‐Arozena Iannis E. Adamopoulos Khosrow Adeli Timon E. Adolph Annagrazia Adornetto Elma Aflaki Galila Agam Anupam Agarwal Bharat B. Aggarwal Maria Agnello Patrizia Agostinis Javed N. Agrewala Alexander Agrotis Patricia V. Aguilar S. Tariq Ahmad Zubair M. Ahmed Ulises Ahumada-Castro Sonja Aits Shu Aizawa Yunus Akkoç Tonia Akoumianaki Hafize Aysin Akpinar Ahmed M. Al‐Abd Lina Al-Akra Abeer Gharaibeh Moulay A. Alaoui‐Jamali Simon Alberti Elísabet Alcocer‐Gómez Cristiano Alessandri Muhammad Ali Md. Abdul Alim Al‐Bari Saeb Aliwaini Javad Alizadeh Eugènia Almacellas Alexandru Almasan Alicia Alonso G. Alonso Nihal Altan‐Bonnet Dario C. Altieri Élida Álvarez Sara Alves Cristine Alvès da Costa Mazen M. Alzaharna Marialaura Amadio Consuelo Amantini Cristina Amaral Susanna Ambrosio Amal O. Amer Veena Ammanathan Zhenyi An Stig Uggerhøj Andersen Shaida A. Andrabi Magaiver Andrade-Silva Allen M. Andres Sabrina Angelini David K. Ann Uche C. Anozie Mohammad Y. Ansari Pedro Antas Adam Antebi Zuriñe Antón Tahira Anwar Lionel Apétoh Nadezda Apostolova Toshiyuki Araki Yasuhiro Araki Kohei Arasaki Wagner L. Araújo Jun Araya Catherine Arden María‐Ángeles Arévalo Sandro Argüelles Esperanza Arias Jyothi Arikkath Hirokazu Arimoto Aileen Ariosa Darius Armstrong‐James Laetitia Pelloquin Ángeles Aroca Daniela S. Arroyo Ivica Arsov Rubén Artero Dalia Maria Lucia Asaro Michael Aschner Milad Ashrafizadeh Osnat Ashur‐Fabian Atanas G. Atanasov Alicia K. Au Patrick Auberger Holger W. Auner Laure Aurelian

In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered field. Our knowledge base relevant new technologies also been expanding. Thus, it is important to formulate on a regular basis updated monitoring autophagy different organisms. Despite numerous reviews, there continues be confusion regarding acceptable methods evaluate autophagy, especially multicellular...

10.1080/15548627.2020.1797280 article EN cc-by-nc-sa Autophagy 2021-01-02

Ochratoxin A (OTA) is a carcinogenic mycotoxin, which produced by Aspergillus and Penicillium genera of fungi commonly contaminates food feed. We others have previously shown that OTA causes sustained activation PI3K/AKT MAPK/ERK1-2 signaling pathways in different cell types animal models. Given the close relationship between cellular activity protein stability, we were curious whether increased may be result OTA-stimulated alterations proteolytic activity. show both major systems,...

10.3390/toxins11110615 article EN cc-by Toxins 2019-10-24

B-cell lymphoma 6 (BCL6) is a transcriptional repressor and oncogenic driver of diffuse large (DLBCL). Here, we report the optimization our previously reported tricyclic quinolinone series for inhibition BCL6. We sought to improve cellular potency in vivo exposure non-degrading isomer, CCT373567, recently published degrader, CCT373566. The major limitation inhibitors was their high topological polar surface areas (TPSA), leading increased efflux ratios. Reducing molecular weight allowed us...

10.1021/acs.jmedchem.3c00155 article EN cc-by Journal of Medicinal Chemistry 2023-04-07

The transcriptional repressor BCL6 is an oncogenic driver found to be deregulated in lymphoid malignancies. Herein, we report the optimization of our previously reported benzimidazolone molecular glue-type degrader CCT369260 CCT373566, a highly potent probe suitable for sustained depletion vivo. We observed sharp degradation SAR, where subtle structural changes conveyed ability induce BCL6. CCT373566 showed modest vivo efficacy lymphoma xenograft mouse model following oral dosing.

10.1021/acs.jmedchem.1c02175 article EN cc-by Journal of Medicinal Chemistry 2022-06-02
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