scholarly journals Correction to: EGFR and BRAF mutations in inverted sinonasal papilloma—a more complex landscape?

2021 ◽  
Author(s):  
Sarah Zonnur ◽  
Andreas Erbersdobler ◽  
Björn Schneider
Author(s):  
Marina Muzza ◽  
Carla Colombo ◽  
Maria Carla Proverbio ◽  
Stefania Rossi ◽  
Delfina Tosi ◽  
...  

Author(s):  
Sara Huerta-Yepez ◽  
S. Ekmekcioglu ◽  
C. M. Rivera-Pazos ◽  
G. Antonio-Andres ◽  
Mario I. Vega ◽  
...  

2020 ◽  
Vol 21 ◽  
Author(s):  
Daniel Sur ◽  
Andrei Havasi ◽  
Alecsandra Gorzo ◽  
Claudia Burz

Background: Anti-EGFR monoclonal antibodies (mAbs) have become a relevant solution for the treatment of patients with metastatic colorectal cancer. Current anti-EGFR monoclonal antibodies face a series of problems, including resistance and non-durable response, and RAS and BRAF mutations serve as exclusion criteria for treatment with anti-EGFR mAbs. Advances in molecular tumor profiling and information on subsequent pathways responsible for disease progression and drug resistance helped develop a new generation of anti-EGFR mAbs. These second-generation mAbs have been developed to overcome existing resistance mechanisms and to limit common side effects. For the moment, existing literature suggests that these novel anti-EGFR mAbs are far from finding their way to clinical practice soon. Objective: In this review, we summarize and evaluate current data regarding ongoing research and completed clinical trials for different second-generation anti-EGFR monoclonal antibodies. Conclusion: Anti-EGFR mAbs exhibit efficacy in advanced colorectal cancer, but second-generation mAbs failed to prove their benefit in the treatment of metastatic colorectal cancer. Understanding the biological basis of primary and acquired drug resistance could allow scientists to design better clinical trials and develop improved second-generation mAbs.


Leukemia ◽  
2020 ◽  
Author(s):  
Courtney E. Hershberger ◽  
Devlin C. Moyer ◽  
Vera Adema ◽  
Cassandra M. Kerr ◽  
Wencke Walter ◽  
...  

Plants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 815
Author(s):  
Sandra V. Rojas-Nossa ◽  
José María Sánchez ◽  
Luis Navarro

Floral development depends on multifactor processes related to genetic, physiological, and ecological pathways. Plants respond to herbivores by activating mechanisms aimed at tolerating, compensating, or avoiding loss of biomass and nutrients, and thereby survive in a complex landscape of interactions. Thus, plants need to overcome trade-offs between development, growth, and reproduction vs. the initiation of anti-herbivore defences. This study aims to assess the frequency of phloem-feeding herbivores in wild populations of the Etruscan honeysuckle (Lonicera etrusca Santi) and study their effects on floral development and reproduction. The incidence of herbivory by the honeysuckle aphid (Hyadaphis passerinii del Guercio) was assessed in three wild populations of the Iberian Peninsula. The effect of herbivory on floral morphology, micromorphology of stigmas and pollen, floral rewards, pollination, and fruit and seed set were studied. The herbivory by aphids reduces the size of flowers and pollen. Additionally, it stops nectar synthesis and causes malformation in pollen and microstructures of stigmas, affecting pollination. As a consequence, fruit set and seed weight are reduced. This work provides evidence of the changes induced by phloem-feeding herbivores in floral development and functioning that affect the ecological processes necessary to maintain the reproductive success of plants.


2021 ◽  
pp. 107815522110055
Author(s):  
Clement Chung

Although therapeutically actionable molecular alterations are widely distributed across many cancer types, only a handful of them show evidence of clinical utility and are recommended for routine clinical practice in the management of cancers of colon and rectum (CRC). This 2021 update aims to provide a succinct summary on the use of prognostic and/or predictive biomarkers (expanded RAS, BRAF, microsatellite-high [MSI-H] or deficient mismatch repair [dMMR], neurotrophic tyrosine receptor kinase [ NTRK] fusion genes, and human epidermal growth factor receptor type II [ HER2] gene amplification) associated with CRC. Therapeutic implications of each relevant predictive or prognostic biomarker for patients with CRC are described, along with discussion on new developments on (1) biomarker-driven therapies such as testing of BRAF, MLH1 promoter methylation and MMR germline genes in differentiating sporadic CRC or hereditary conditions such as Lynch syndrome; (2) first-line use of immune checkpoint inhibitors in metastatic CRC; (3) risk stratification and therapy selection based on primary tumor location (left-sided vs. right-sided colon cancer); (3) atypical BRAF mutations; (4) use of EGFR directed therapy in the perioperative oligometastatic disease setting; (5) re-challenge of EGFR directed therapy and (6) personalizing therapy of fluoropyrimidine and irinotecan based on new evidence in pharmacogenomic testing. Data are collected and analyzed from available systematic reviews and meta-analyses of treatments with known therapeutic targets in CRC, which may be associated with predictive and/or prognostic biomarkers. Discussions are presented in an application-based format, with goal to empower pharmacists or other clinicians to gain awareness and understanding in biomarker-driven cancer therapy issues.


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