Vaping and Lung Cancer – A Review of Current Data and Recommendations

Lung Cancer ◽  
2021 ◽  
Author(s):  
Dara Bracken-Clarke ◽  
Dhruv Kapoor ◽  
Anne Marie Baird ◽  
Paul James Buchanan ◽  
Kathy Gately ◽  
...  
Keyword(s):  
2020 ◽  
Vol 10 (1) ◽  
pp. 108-122
Author(s):  
Joanna Pancewicz

Non-small cell lung cancer is one of the most commonly diagnosed cancer with a very high mortality rate. Trying to understand the mechanisms underlying the progression of this type of cancer, it is necessary to evaluate the changes occurring at molecular level in cancer cells. Besides the widely studied signaling pathways and genes which are dysregulated in NSCLC, there is a large group of non-coding RNAs involved in cancer pathogenesis. Those RNAs are tissue specific heterogeneous class of RNAs that play many functions in physiological condition in cells, nevertheless current data has shown that lncRNAs are also functional in different types of cancer. Moreover, it has been suggest that lncRNAs are involved in cancer progression by controlling key signaling pathways involved in diverse types of tumors. Notch signaling is one of those pathways, very often deregulated in NSCLC. Therefore in this review I summarized recent outcomes according the importance of lncRNAs in regulation of Notch pathway in the pathogenesis of NSCLC.


Author(s):  
R.I. Bersimbaev ◽  
◽  
O.V. Bulgakova ◽  
A.A. Aripova ◽  
A.Zh. Kausbekova ◽  
...  

Exosomes are extracellular vesicles secreted by almost all cell types that can function as a cell-to-cell carrier of information, providing pleiotropic functions in intercellular communication. Exosomes can transport various biomolecules, including proteins and nucleic acids, into recipient cells. The review analyzed the current data on the role of exosomes and the possibility of using exosomal microRNAs as a biomarker in the diagnosis of lung cancer. MicroRNAs can act as oncogenes or tumor suppressors, so they can regulate the expression of genes that play an important role in oncogenesis. At the moment, microRNAs of exosomes are one of the main candidates for the role of molecular markers in liquid biopsy for the diagnosis of oncological diseases. The review analyzes the diagnostic potential of the use of exosomes in carcinogenesis in general, with an emphasis on the use of exosomal microRNAs as biomarkers of lung cancer.


2003 ◽  
Vol 4 (4) ◽  
pp. 210-212 ◽  
Author(s):  
Heather DeGrendele ◽  
Chandra P. Belani ◽  
Harvey Pass

2020 ◽  
Vol 8 (2) ◽  
pp. e000971
Author(s):  
Alex Friedlaender ◽  
Stephen V Liu ◽  
Alfredo Addeo

Immune-checkpoint inhibitors have deeply changed the therapeutic landscape of advanced non-small cell lung cancer without actionable genomic alterations. Immune-checkpoint inhibitors have become standard front-line therapy, especially among patients with tumours expressing high levels of programmed death ligand-1; yet, many patients do not respond to therapy. This has led to the adoption of front-line combination therapies, administering programmed death-1 inhibitors concomitantly either with other checkpoint inhibitors, chemotherapy or both. Today’s approved standard of care includes options with chemoimmunotherapy or dual checkpoint blockade, but each combination has only been compared to chemotherapy alone and no head-to-head trials exist. In cross-trial comparisons, combinations trials appear to show numerically superior responses to single-agent checkpoint inhibitors but the question is whether they ultimately offer a survival advantage. In this manuscript, we summarize and analyse all currently available front-line immune-checkpoint inhibitor trials in non-small cell lung cancer, whether as monotherapy or in combination with chemotherapy, second immunotherapy agents or both. Should standards of care change given the current data? While we ponder this question, we illustrate current data and conclude that the answer lies in tracking the tail of the survival curves.


2004 ◽  
Vol 5 (6) ◽  
pp. 337-339
Author(s):  
G. Kesava Reddy ◽  
Chandra P. Belani ◽  
Vinay K. Jain ◽  
Michael C. Perry

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