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1.
Modulation by flavonoids of cell multidrug resistance mediated by P-glycoprotein and related ABC transporters 总被引:9,自引:0,他引:9
Di Pietro A Conseil G Pérez-Victoria JM Dayan G Baubichon-Cortay H Trompier D Steinfels E Jault JM de Wet H Maitrejean M Comte G Boumendjel A Mariotte AM Dumontet C McIntosh DB Goffeau A Castanys S Gamarro F Barron D 《Cellular and molecular life sciences : CMLS》2002,59(2):307-322
Cancer cell resistance to chemotherapy is often mediated by overexpression of P-glycoprotein, a plasma membrane ABC (ATP-binding cassette) transporter which extrudes cytotoxic drugs at the expense of ATP hydrolysis. P-glycoprotein (ABCB1, according to the human gene nomenclature committee) consists of two homologous halves each containing a transmembrane domain (TMD) involved in drug binding and efflux, and a cytosolic nucleotide-binding domain (NBD) involved in ATP binding and hydrolysis, with an overall (TMD-NBD)2 domain topology. Homologous ABC multidrug transporters, from the same ABCB family, are found in many species such as Plasmodiumfalciparum and Leishmania spp. protozoa, where they induce resistance to antiparasitic drugs. In yeasts, some ABC transporters involved in resistance to fungicides, such as Saccharomyces cerevisiae Pdr5p and Snq2p, display a different (NBD-TMD)2 domain topology and are classified in another family, ABCG. Much effort has been spent to modulate multidrug resistance in the different species by using specific inhibitors, but generally with little success due to additional cellular targets and/or extrusion of the potential inhibitors. This review shows that due to similarities in function and maybe in three-dimensional organization of the different transporters, common potential modulators have been found. An in vitro 'rational screening' was performed among the large flavonoid family using a four-step procedure: (i) direct binding to purified recombinant cytosolic NBD and/or full-length transporter, (ii) inhibition of ATP hydrolysis and energy-dependent drug interaction with transporter-enriched membranes, (iii) inhibition of cell transporter activity monitored by flow cytometry and (iv) chemosensitization of cell growth. The results indicate that prenylated flavonoids bind with high affinity, and strongly inhibit drug interaction and nucleotide hydrolysis. As such, they constitute promising potential modulators of multidrug resistance. 相似文献
2.
Lage H 《Cellular and molecular life sciences : CMLS》2008,65(20):3145-3167
Although various mechanisms involved in anticancer multidrug resistance (MDR) can be identified, it remains a major problem
in oncology. Beyond that, the introduction of new “targeted” drugs have not solved the problem. On the contrary, it has been
demonstrated that the “classical” MDR-associated mechanisms are similar or identical to those causing resistance to these
novel agents. These mechanisms include the enhanced activity of drug pumps, i.e. ABC or alternative transporters; modulation
of cellular death pathways; alteration and repair of target molecules; and various less common mechanisms. Together they build
a complex network of cellular pathways and molecular mechanisms mediating an individual MDR phenotype. Although the application
of new high throughput “-omics” technologies have identified multiple new gene-/protein expression signatures or factors associated
with drug resistance, so far none of these findings has been useful for creating improved diagnostic assays, for prediction
of individual therapy response, or for development of updated chemosensitizers.
Received 05 March 2008; received after revision 21 May 2008; accepted 23 May 2008 相似文献
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From MDR to MXR: new understanding of multidrug resistance systems, their properties and clinical significance 总被引:31,自引:0,他引:31
Litman T Druley TE Stein WD Bates SE 《Cellular and molecular life sciences : CMLS》2001,58(7):931-959
The ATP binding cassette (ABC) superfamily of membrane transporters is one of the largest protein classes known, and counts numerous proteins involved in the trafficking of biological molecules across cell membranes. The first known human ABC transporter was P-glycoprotein (P-gp), which confers multidrug resistance (MDR) to anticancer drugs. In recent years, we have obtained an increased understanding of the mechanism of action of P-gp as its ATPase activity, substrate specificity and pharmacokinetic interactions have been investigated. This review focuses on the functional characterization of P-gp, as well as other ABC transporters involved in MDR: the family of multidrug-resistance-associated proteins (MRP1-7), and the recently discovered ABC half-transporter MXR (also known as BCRP, ABCP and ABCG2). We describe recent progress in the analysis of protein structure-function relationships, and consider the conceptual problem of defining and identifying substrates and inhibitors of MDR. An in-depth discussion follows of how coupling of nucleotide hydrolysis to substrate transport takes place, and we propose a scheme for the mechanism of P-gp function. Finally, the clinical correlations, both for reversal of MDR in cancer and for drug delivery, are discussed. 相似文献
5.
Henriikka Kentala Annika Koponen Helena Vihinen Juho Pirhonen Gerhard Liebisch Zoltan Pataj Annukka Kivelä Shiqian Li Leena Karhinen Eeva Jääskeläinen Robert Andrews Leena Meriläinen Silke Matysik Elina Ikonen You Zhou Eija Jokitalo Vesa M. Olkkonen 《Cellular and molecular life sciences : CMLS》2018,75(21):4041-4057
ORP2 is a ubiquitously expressed OSBP-related protein previously implicated in endoplasmic reticulum (ER)—lipid droplet (LD) contacts, triacylglycerol (TG) metabolism, cholesterol transport, adrenocortical steroidogenesis, and actin-dependent cell dynamics. Here, we characterize the role of ORP2 in carbohydrate and lipid metabolism by employing ORP2-knockout (KO) hepatoma cells (HuH7) generated by CRISPR-Cas9 gene editing. The ORP2-KO and control HuH7 cells were subjected to RNA sequencing, analyses of Akt signaling, carbohydrate and TG metabolism, the extracellular acidification rate, and the lipidome, as well as to transmission electron microscopy. The loss of ORP2 resulted in a marked reduction of active phosphorylated Akt(Ser473) and its target Glycogen synthase kinase 3β(Ser9), consistent with defective Akt signaling. ORP2 was found to form a physical complex with the key controllers of Akt activity, Cdc37, and Hsp90, and to co-localize with Cdc37 and active Akt(Ser473) at lamellipodial plasma membrane regions, in addition to the previously reported ER–LD localization. ORP2-KO reduced glucose uptake, glycogen synthesis, glycolysis, mRNA-encoding glycolytic enzymes, and SREBP-1 target gene expression, and led to defective TG synthesis and storage. ORP2-KO did not reduce but rather increased ER–LD contacts under basal culture conditions and interfered with their expansion upon fatty acid loading. Together with our recently published work (Kentala et al. in FASEB J 32:1281–1295, 2018), this study identifies ORP2 as a new regulatory nexus of Akt signaling, cellular energy metabolism, actin cytoskeletal function, cell migration, and proliferation. 相似文献
6.
K. Berneis W. Bollag M. Kofler H. Lüthy 《Cellular and molecular life sciences : CMLS》1965,21(6):318-320
Zusammenfassung Die kombinierte Einwirkung von ionisierender Strahlung und N-Isopropyl-p-(2-methyl-hydrazinomethyl)benzamid hydrochlorid (Natulan®) führt zu einem wesentlich stärkeren Abbau von Desoxyribonucleinsäure (DNS) als auf Grund der linearen Superposition zu erwarten wäre. Der Synergismus ist am ausgeprägtesten, wenn der Zusatz von Natulan unmittelbar nach der Bestrahlung erfolgt. Dieser Effekt kann als Folge der Bildung instabiler Peroxide während der Bestrahlung erklärt werden. Bekanntlich zerfallen die bei der Bestrahlung entstandenen organischen Peroxide zum grössten Teil innerhalb der ersten zwei bis drei Stunden nach der Bestrahlung unter Bildung freier Radikale. Diese können als Startradikale bei der Autoxydation von Natulan wirken und daher den Abbau von DNS beschleunigen. 相似文献
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N. Soltani S. Chebira J. P. Delbecque J. Delachambre 《Cellular and molecular life sciences : CMLS》1993,49(12):1088-1091
Flucycloxuron, a novel benzoylphenylurea (BPU) derivative, exhibited insecticidal activity when injected into newly ecdysed pupae ofTenebrio molitor. Mortality occurs because of defective adult ecdysis. Treatment caused a reduction in both cuticle thickness and incorporation of14C-labelled precursor into chitin, although it had no significant effect on the protein synthesis. The potencies of other BPU compounds as inhibitors of chitin biosynthesis have been examined and results showed that diflubenzuron was less effective than either flucycloxuron or triflumuron. 相似文献
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Frédérique Nolin Jean Michel Laurence Wortham Pavel Tchelidze Gérard Balossier Vincent Banchet Hélène Bobichon Nathalie Lalun Christine Terryn Dominique Ploton 《Cellular and molecular life sciences : CMLS》2013,70(13):2383-2394
The cell is a crowded volume, with estimated mean mass percentage of macromolecules and of water ranging from 7.5 to 45 and 55 to 92.5 %, respectively. However, the concentrations of macromolecules and water at the nanoscale within the various cell compartments are unknown. We recently developed a new approach, correlative cryo-analytical scanning transmission electron microscopy, for mapping the quantity of water within compartments previously shown to display GFP-tagged protein fluorescence on the same ultrathin cryosection. Using energy-dispersive X-ray spectrometry (EDXS), we then identified various elements (C, N, O, P, S, K, Cl, Mg) in these compartments and quantified them in mmol/l. Here, we used this new approach to quantify water and elements in the cytosol, mitochondria, condensed chromatin, nucleoplasm, and nucleolar components of control and stressed cancerous cells. The water content of the control cells was between 60 and 83 % (in the mitochondria and nucleolar fibrillar centers, respectively). Potassium was present at concentrations of 128–462 mmol/l in nucleolar fibrillar centers and condensed chromatin, respectively. The induction of nucleolar stress by treatment with a low dose of actinomycin-D to inhibit rRNA synthesis resulted in both an increase in water content and a decrease in the elements content in all cell compartments. We generated a nanoscale map of water and elements within the cell compartments, providing insight into their changes induced by nucleolar stress. 相似文献
11.
AMP-activated protein kinase in skeletal muscle: From structure and localization to its role as a master regulator of cellular metabolism 总被引:1,自引:0,他引:1
Witczak CA Sharoff CG Goodyear LJ 《Cellular and molecular life sciences : CMLS》2008,65(23):3737-3755
The AMP-activated protein kinase (AMPK) is a metabolite sensing serine/threonine kinase that has been termed the master regulator
of cellular energy metabolism due to its numerous roles in the regulation of glucose, lipid, and protein metabolism. In this
review, we first summarize the current literature on a number of important aspects of AMPK in skeletal muscle. These include
the following: (1) the structural components of the three AMPK subunits (i.e. AMPKα, β, and γ), and their differential localization
in response to stimulation in muscle; (2) the biochemical regulation of AMPK by AMP, protein phosphatases, and its three known
upstream kinases, LKB1, Ca2+/calmodulin-dependent protein kinase kinase (CaMKK), and transforming growth factor-β-activated kinase 1 (TAK1); (3) the pharmacological
agents that are currently available for the activation and inhibition of AMPK; (4) the physiological stimuli that activate
AMPK in muscle; and (5) the metabolic processes that AMPK regulates in skeletal muscle.
Received 04 May 2008; received after revision 14 June 2008; accepted 14 July 2008 相似文献
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Comparison of SXT and R391, two conjugative integrating elements: definition of a genetic backbone for the mobilization of resistance determinants 总被引:10,自引:0,他引:10
Beaber JW Burrus V Hochhut B Waldor MK 《Cellular and molecular life sciences : CMLS》2002,59(12):2065-2070
The SXT element (SXT) is becoming an increasingly prevalent vector for the dissemination of antibiotic resistances in Vibrio cholerae. SXT is a member of a larger family of elements, formerly defined as IncJ plasmids, that are self-transmissible by conjugation
and integrate site-specifically into the host chromosome. Comparison of the DNA sequences of SXT and R391, an IncJ element
from Providencia rettgeri, indicate that these elements consist of a conserved backbone that mediates the regulation, excision/integration and conjugative
transfer of the elements. Both elements have insertions into this backbone that either confer the element-specific properties
or are of unknown function. Interestingly, the conserved SXT and R391 backbone apparently contains hotspots for insertion
of additional DNA sequences. This backbone represents a scaffold for the mobilization of genetic material between a wide range
of Gram-negative bacteria, allowing for rapid adaptation to changing envi
ronments.
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ID="*"Corresponding author. 相似文献
14.
Sarno S Mazzorana M Traynor R Ruzzene M Cozza G Pagano MA Meggio F Zagotto G Battistutta R Pinna LA 《Cellular and molecular life sciences : CMLS》2012,69(3):449-460
8-hydroxy-4-methyl-9-nitrobenzo(g)chromen-2-one (NBC) has been found to be a fairly potent ATP site-directed inhibitor of
protein kinase CK2 (Ki = 0.22 μM). Here, we show that NBC also inhibits PIM kinases, especially PIM1 and PIM3, the latter
as potently as CK2. Upon removal of the nitro group, to give 8-hydroxy-4-methyl-benzo(g)chromen-2-one (here referred to as
“denitro NBC”, dNBC), the inhibitory power toward CK2 is almost entirely lost (IC50 > 30 μM) whereas that toward PIM1 and PIM3 is maintained; in addition, dNBC is a potent inhibitor of a number of other kinases
that are weakly inhibited or unaffected by NBC, with special reference to DYRK1A whose IC50 values with NBC and dNBC are 15 and 0.60 μM, respectively. Therefore, the observation that NBC, unlike dNBC, is a potent
inducer of apoptosis is consistent with the notion that this effect is mediated by inhibition of endogenous CK2. The structural
features underlying NBC selectivity have been revealed by inspecting its 3D structure in complex with the catalytic subunit
of Z. mays CK2. The crucial role of the nitro group is exerted both through a direct electrostatic interaction with the side chain of Lys68
and, indirectly, by enhancing the acidic dissociation constant of the adjacent hydroxyl group which interacts with a conserved
water molecule in the deepest part of the cavity. By contrast, the very same nitro group is deleterious for the binding to
the active site of DYRK1A, as disclosed by molecular docking. This provides the rationale for preferential inhibition of DYRK1A
by dNBC. 相似文献
15.
GPR39 is a vertebrate G protein-coupled receptor related to the ghrelin/neurotensin receptor subfamily. The receptor is expressed
in a range of tissues including the pancreas, gut/gastrointestinal tract, liver, kidney and in some regions of the brain.
GPR39 was initially thought to be the cognitive receptor for the peptide hormone, obestatin. However, subsequent in vitro
studies have failed to demonstrate binding of this peptide to the receptor. Zn2+ has been shown to be a potent stimulator of GPR39 activity via the Gαq, Gα12/13 and Gαs pathways. The potency and specificity of Zn2+ in activating GPR39 suggest it to be a physiologically important agonist. GPR39 is now emerging as an important transducer
of autocrine and paracrine Zn2+ signals, impacting upon cellular processes such as insulin secretion, gastric emptying, neurotransmission and epithelial
repair. This review focuses on the molecular, structural and biological properties of GPR39 and its various physiological
functions. 相似文献