Purpose: The aim of the study was to verify the hypothesis that the cMet oncogene is implicated in chemio-and novel drug resistance in multiple myeloma.Experimental Design: We have evaluated the expression levels of cMET/phospho-cMET (p-cMET) and the activity of the novel selective p-cMET inhibitor (SU11274) in multiple myeloma cells, either sensitive (RPMI-8226 and MM.1S) or resistant (R5 and MM.1R) to anti-multiple myeloma drugs, in primary plasma cells and in multiple myeloma xenograft models.Results: We found that resistant R5 and MM.1R cells presented with higher cMET phosphorylation, thus leading to constitutive activation of cMET-dependent signaling pathways. R5 cells exhibited a higher susceptibility to the SU11274 inhibitory effects on viability, proliferation, chemotaxis, adhesion, and to its apoptogenic effects. SU11274 was able to revert drug resistance in R5 cells. R5 but not RPMI-8226 cells displayed cMET-dependent activation of mitogen-activated protein kinase pathway. The cMET and p-cMET expression was higher on plasma cells from patients with multiple myeloma at relapse or on drug resistance than on those from patients at diagnosis, complete/partial remission, or from patients with monoclonal gammopathy of unknown significance. Viability, chemotaxis, adhesion to fibronectin or paired bone marrow stromal cells of plasma cells from relapsed or resistant patients was markedly inhibited by SU11274. Importantly, SU11274 showed higher therapeutic activity in R5-than in RPMI-8226-induced plasmocytomas. In R5 tumors, it caused apoptosis and necrosis and reverted bortezomib resistance.Conclusion: Our findings suggest that the cMET pathway is constitutively activated in relapsed and resistant multiple myeloma where it may also be responsible for induction of drug resistance, thus providing the preclinical rationale for targeting cMET in patients with relapsed/refractory multiple myeloma.
Sequential pattern mining is a computationally challenging task since algorithms have to generate and/or test a combinatorially explosive number of intermediate subsequences. In order to reduce complexity, some researchers focus on the task of mining closed sequential patterns. This not only results in increased efficiency, but also provides a way to compact results, while preserving the same expressive power of patterns extracted by means of traditional (non-closed) sequential pattern mining algorithms. In this paper, we present CloFAST, a novel algorithm for mining closed frequent sequences of itemsets. It combines a new data representation of the dataset, based on sparse id-lists and vertical id-lists, whose theoretical properties are studied in order to fast count the support of sequential patterns, with a novel one-step technique both to check sequence closure and to prune the search space. Contrary to almost all the existing algorithms, which iteratively alternate itemset extension and sequence extension, CloFAST proceeds in two steps. Initially, all closed frequent itemsets are mined in order to obtain an initial set of sequences of size 1. Then, new sequences are generated by directly working on the sequences, without mining additional frequent itemsets. A thorough performance study with both real-world and artificially generated datasets empirically proves that CloFAST outperforms the state-of-the-art algorithms, both in time and memory consumption, especially when mining long closed sequences
In this paper, we tackle the problem of power prediction of several photovoltaic (PV) plants spread over an extended geographic area and connected to a power grid. The paper is intended to be a comprehensive study of one-day ahead forecast of PV energy production along several dimensions of analysis: i) The consideration of the spatio-temporal autocorrelation, which characterizes geophysical phenomena, to obtain more accurate predictions. ii) The learning setting to be considered, i.e. using simple output prediction for each hour or structured output prediction for each day. iii) The learning algorithms: We compare artificial neural networks, most often used for PV prediction forecast, and regression trees for learning adaptive models. The results obtained on two PV power plant datasets show that: taking into account spatio/temporal autocorrelation is beneficial; the structured output prediction setting significantly outperforms the non-structured output prediction setting; and regression trees provide better models than artificial neural networks.
Sequential pattern mining is an important data mining task with applications in basket analysis, world wide web, medicine and telecommunication. This task is challenging because sequence databases are usually large with many and long sequences and the number of possible sequential patterns to mine can be exponential. We proposed a new sequential pattern mining algorithm called FAST which employs a representation of the dataset with indexed sparse id-lists to fast counting the support of sequential patterns. We also use a lexicographic tree to improve the efficiency of candidates generation. FAST mines the complete set of patterns by greatly reducing the effort for support counting and candidate sequences generation. Experimental results on artificial and real data show that our method outperforms existing methods in literature up to an order of magnitude or two for large datasets
The discovery and extraction of general lists on the Web continues to be an important problem facing the Web mining community.\ud There have been numerous studies that claim to automatically extract\ud structured data (i.e. lists, record sets, tables, etc.) from the Web for various purposes. Our own recent experiences have shown\ud that the list-finding methods used as part of these larger frameworks do not generalize well and therefore ought to be reevaluated. This paper briefly describes some of the current approaches, and tests\ud them on various list-pages. Based on our findings, we conclude that analyzing a Web page’s DOM-structure is not sufficient for the general list finding task
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
334 Leonard St
Brooklyn, NY 11211
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.