Contribution of CXCR3-mediated signaling in the metastatic cascade of solid malignancies

2021 ◽  
Vol 1876 (2) ◽  
pp. 188628
Author(s):  
Andrew Cannon ◽  
Christopher M. Thompson ◽  
Rakesh Bhatia ◽  
Rakhee R.K. Kandy ◽  
Joyce C. Solheim ◽  
...  
Author(s):  
Khalaf Kridin ◽  
Rimma Laufer Britva ◽  
Dana Tzur Bitan ◽  
Giovanni Damiani ◽  
Arnon D Cohen

2017 ◽  
Vol 22 (1) ◽  
pp. 53-60 ◽  
Author(s):  
Jin Sheng ◽  
Ya‐Xiong Zhang ◽  
Xiao‐Bo He ◽  
Wen‐Feng Fang ◽  
Yun‐Peng Yang ◽  
...  

Author(s):  
Shuyang Yao ◽  
Filip Janku ◽  
Vivek Subbiah ◽  
John Stewart ◽  
Sapna Pradyuman Patel ◽  
...  

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Jillian Hattaway Luttman ◽  
Ashley Colemon ◽  
Benjamin Mayro ◽  
Ann Marie Pendergast

AbstractThe ABL kinases, ABL1 and ABL2, promote tumor progression and metastasis in various solid tumors. Recent reports have shown that ABL kinases have increased expression and/or activity in solid tumors and that ABL inactivation impairs metastasis. The therapeutic effects of ABL inactivation are due in part to ABL-dependent regulation of diverse cellular processes related to the epithelial to mesenchymal transition and subsequent steps in the metastatic cascade. ABL kinases target multiple signaling pathways required for promoting one or more steps in the metastatic cascade. These findings highlight the potential utility of specific ABL kinase inhibitors as a novel treatment paradigm for patients with advanced metastatic disease.


Author(s):  
Kamal S. Saini ◽  
Chris Twelves

AbstractThe complexity of neoplasia and its treatment are a challenge to the formulation of general criteria that are applicable across solid cancers. Determining the number of prior lines of therapy (LoT) is critically important for optimising future treatment, conducting medication audits, and assessing eligibility for clinical trial enrolment. Currently, however, no accepted set of criteria or definitions exists to enumerate LoT. In this article, we seek to open a dialogue to address this challenge by proposing a systematic and comprehensive framework to determine LoT uniformly across solid malignancies. First, key terms, including LoT and ‘clinical progression of disease’ are defined. Next, we clarify which therapies should be assigned a LoT, and why. Finally, we propose reporting LoT in a novel and standardised format as LoT N (CLoT + PLoT), where CLoT is the number of systemic anti-cancer therapies (SACT) administered with curative intent and/or in the early setting, PLoT is the number of SACT given with palliative intent and/or in the advanced setting, and N is the sum of CLoT and PLoT. As a next step, the cancer research community should develop and adopt standardised guidelines for enumerating LoT in a uniform manner.


Sign in / Sign up

Export Citation Format

Share Document