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Challenges and Opportunities in Cancer Drug Resistance.
Ward, Richard A; Fawell, Stephen; Floc'h, Nicolas; Flemington, Vikki; McKerrecher, Darren; Smith, Paul D.
Afiliación
  • Ward RA; Medicinal Chemistry, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, U.K.
  • Fawell S; Oncology R&D, AstraZeneca, Waltham, Massachusetts 02451, United States.
  • Floc'h N; Bioscience, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, U.K.
  • Flemington V; Bioscience, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, U.K.
  • McKerrecher D; Medicinal Chemistry, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, U.K.
  • Smith PD; Bioscience, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, U.K.
Chem Rev ; 121(6): 3297-3351, 2021 03 24.
Article en En | MEDLINE | ID: mdl-32692162
ABSTRACT
There has been huge progress in the discovery of targeted cancer therapies in recent years. However, even for the most successful and impactful cancer drugs which have been approved, both innate and acquired mechanisms of resistance are commonplace. These emerging mechanisms of resistance have been studied intensively, which has enabled drug discovery scientists to learn how it may be possible to overcome such resistance in subsequent generations of treatments. In some cases, novel drug candidates have been able to supersede previously approved agents; in other cases they have been used sequentially or in combinations with existing treatments. This review summarizes the current field in terms of the challenges and opportunities that cancer resistance presents to drug discovery scientists, with a focus on small molecule therapeutics. As part of this review, common themes and approaches have been identified which have been utilized to successfully target emerging mechanisms of resistance. This includes the increase in target potency and selectivity, alternative chemical scaffolds, change of mechanism of action (covalents, PROTACs), increases in blood-brain barrier permeability (BBBP), and the targeting of allosteric pockets. Finally, wider approaches are covered such as monoclonal antibodies (mAbs), bispecific antibodies, antibody drug conjugates (ADCs), and combination therapies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoconjugados / Anticuerpos Monoclonales / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Chem Rev Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoconjugados / Anticuerpos Monoclonales / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Chem Rev Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido