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Google Duo to allow users to make video calls on Chrome




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How to speed up and tweak Chrome browser performance on mobile devices

  When it comes to choosing a browser for your android device, chrome is a no-brainer. Here are a few tips to make your experience even better: Preload webpages Chrome can help you render webpages f...





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Google Chrome 80.0.3987.87 Denial Of Service

Google Chrome version 80.0.3987.87 heap-corruption remote denial of service proof of concept exploit.





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Google Chrome 80 JSCreate Side-Effect Type Confusion

This Metasploit module exploits an issue in Google Chrome version 80.0.3987.87 (64 bit). The exploit corrupts the length of a float array (float_rel), which can then be used for out of bounds read and write on adjacent memory. The relative read and write is then used to modify a UInt64Array (uint64_aarw) which is used for read and writing from absolute memory. The exploit then uses WebAssembly in order to allocate a region of RWX memory, which is then replaced with the payload shellcode. The payload is executed within the sandboxed renderer process, so the browser must be run with the --no-sandbox option for the payload to work correctly.















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NoScript Extension Officially Released For Google Chrome





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Google Chrome To Block Heavy Ads That Use Too Many Resources













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Acetaminophen-Induced Liver Injury Alters Expression and Activities of Cytochrome P450 Enzymes in an Age-Dependent Manner in Mouse Liver [Articles]

Drug-induced liver injury (DILI) is a global medical problem. The risk of DILI is often related to expression and activities of drug-metabolizing enzymes, especially cytochrome P450s (P450s). However, changes on expression and activities of P450s after DILI have not been determined. The aim of this study is to fill this knowledge gap. Acetaminophen (APAP) was used as a model drug to induce DILI in C57BL/6J mice at different ages of days 10 (infant), 22 (child), and 60 (adult). DILI was assessed by levels of alanine aminotransferase and aspartate aminotransferase in plasma with a confirmation by H&E staining on liver tissue sections. The expression of selected P450s at mRNA and protein levels was measured by real-time polymerase chain reaction and liquid chromatography–tandem mass spectrometry, respectively. The activities of these P450s were determined by the formation of metabolites from probe drugs for each P450 using ultraperformance liquid chromatography–quadrupole time of flight mass spectrometry. DILI was induced at mild to severe levels in a dose-dependent manner in 200, 300, and 400 mg/kg APAP-treated groups at child and adult ages, but not at the infant age. Significantly decreased expression at mRNA and protein levels as well as enzymatic activities of CYP2E1, 3A11, 1A2, and 2C29 were found at child and adult ages. Adult male mice were more susceptible to APAP-induced liver injury than female mice with more decreased expression of P450s. These results suggest that altered levels of P450s in livers severely injured by drugs may affect the therapeutic efficacy of drugs, which are metabolized by P450s, more particularly for males.

SIGNIFICANCE STATEMENT

The current study in an animal model demonstrates that acetaminophen-induced liver injury results in decreased expression and enzyme activities of several examined drug-metabolizing cytochrome P450s (P450s). The extent of such decreases is correlated to the degree of liver injury severity. The generated data may be translated to human health for patients who have drug-induced liver injury with decreased capability to metabolize drugs by certain P450s.




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Spectral and photochemical diversity of tandem cysteine cyanobacterial phytochromes [Plant Biology]

The atypical trichromatic cyanobacterial phytochrome NpTP1 from Nostoc punctiforme ATCC 29133 is a linear tetrapyrrole (bilin)-binding photoreceptor protein that possesses tandem-cysteine residues responsible for shifting its light-sensing maximum to the violet spectral region. Using bioinformatics and phylogenetic analyses, here we established that tandem-cysteine cyanobacterial phytochromes (TCCPs) compose a well-supported monophyletic phytochrome lineage distinct from prototypical red/far-red cyanobacterial phytochromes. To investigate the light-sensing diversity of this family, we compared the spectroscopic properties of NpTP1 (here renamed NpTCCP) with those of three phylogenetically diverged TCCPs identified in the draft genomes of Tolypothrix sp. PCC7910, Scytonema sp. PCC10023, and Gloeocapsa sp. PCC7513. Recombinant photosensory core modules of ToTCCP, ScTCCP, and GlTCCP exhibited violet-blue–absorbing dark-states consistent with dual thioether-linked phycocyanobilin (PCB) chromophores. Photoexcitation generated singly-linked photoproduct mixtures with variable ratios of yellow-orange and red-absorbing species. The photoproduct ratio was strongly influenced by pH and by mutagenesis of TCCP- and phytochrome-specific signature residues. Our experiments support the conclusion that both photoproduct species possess protonated 15E bilin chromophores, but differ in the ionization state of the noncanonical “second” cysteine sulfhydryl group. We found that the ionization state of this and other residues influences subsequent conformational change and downstream signal transmission. We also show that tandem-cysteine phytochromes present in eukaryotes possess similar amino acid substitutions within their chromophore-binding pocket, which tune their spectral properties in an analogous fashion. Taken together, our findings provide a roadmap for tailoring the wavelength specificity of plant phytochromes to optimize plant performance in diverse natural and artificial light environments.




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CXL146, a Novel 4H-Chromene Derivative, Targets GRP78 to Selectively Eliminate Multidrug-Resistant Cancer Cells [Articles]

The 78-kDa glucose-regulated protein (GRP78), an endoplasmic reticulum (ER) chaperone, is a master regulator of the ER stress. A number of studies revealed that high levels of GRP78 protein in cancer cells confer multidrug resistance (MDR) to therapeutic treatment. Therefore, drug candidate that reduces GRP78 may represent a novel approach to eliminate MDR cancer cells. Our earlier studies showed that a set of 4H-chromene derivatives induced selective cytotoxicity in MDR cancer cells. In the present study, we elucidated its selective mechanism in four MDR cancer cell lines with one lead candidate (CXL146). Cytotoxicity results confirmed the selective cytotoxicity of CXL146 toward the MDR cancer cell lines. We noted significant overexpression of GRP78 in all four MDR cell lines compared with the parental cell lines. Unexpectedly, CXL146 treatment rapidly and dose-dependently reduced GRP78 protein in MDR cancer cell lines. Using human leukemia (HL) 60/mitoxantrone (MX) 2 cell line as the model, we demonstrated that CXL146 treatment activated the unfolded protein response (UPR); as evidenced by the activation of inositol-requiring enzyme 1α, protein kinase R–like ER kinase, and activating transcription factor 6. CXL146-induced UPR activation led to a series of downstream events, including extracellular signal-regulated kinase 1/2 and c-Jun N-terminal kinase activation, which contributed to CXL146-induced apoptosis. Targeted reduction in GRP78 resulted in reduced sensitivity of HL60/MX2 toward CXL146. Long-term sublethal CXL146 exposure also led to reduction in GRP78 in HL60/MX2. These data collectively support GRP78 as the target of CXL146 in MDR treatment. Interestingly, HL60/MX2 upon long-term sublethal CXL146 exposure regained sensitivity to mitoxantrone treatment. Therefore, further exploration of CXL146 as a novel therapy in treating MDR cancer cells is warranted.

SIGNIFICANCE STATEMENT

Multidrug resistance is one major challenge to cancer treatment. This study provides evidence that cancer cells overexpress 78-kDa glucose-regulated protein (GRP78) as a mechanism to acquire resistance to standard cancer therapies. A chromene-based small molecule, CXL146, selectively eliminates cancer cells with GRP78 overexpression via activating unfolded protein response–mediated apoptosis. Further characterization indicates that CXL146 and standard therapies complementarily target different populations of cancer cells, supporting the potential of CXL146 to overcome multidrug resistance in cancer treatment.




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Oxidative Catabolism of (+)-Pinoresinol Is Initiated by an Unusual Flavocytochrome Encoded by Translationally Coupled Genes within a Cluster of (+)-Pinoresinol-Coinduced Genes in Pseudomonas sp. Strain SG-MS2 [Biodegradation]

Burkholderia sp. strain SG-MS1 and Pseudomonas sp. strain SG-MS2 have previously been found to mineralize (+)-pinoresinol through a common catabolic pathway. Here, we used comparative genomics, proteomics, protein semipurification, and heterologous expression to identify a flavoprotein from the vanillyl alcohol oxidase/p-cresol methyl hydroxylase (VAO/PCMH) enzyme family in SG-MS2 that carries out the initial hydroxylation of (+)-pinoresinol at the benzylic carbon. The cognate gene is translationally coupled with a downstream cytochrome gene, and the cytochrome is required for activity. The flavoprotein has a unique combination of cofactor binding and cytochrome requirements for the VAO/PCMH family. The heterologously expressed enzyme has a Km of 1.17 μM for (+)-pinoresinol. The enzyme is overexpressed in strain SG-MS2 upon exposure to (+)-pinoresinol, along with 45 other proteins, 22 of which were found to be encoded by genes in an approximately 35.1-kb cluster also containing the flavoprotein and cytochrome genes. Homologs of 18 of these 22 genes, plus the flavoprotein and cytochrome genes, were also found in a 38.7-kb cluster in SG-MS1. The amino acid identities of four of the other proteins within the SG-MS2 cluster suggest they catalyze conversion of hydroxylated pinoresinol to protocatechuate and 2-methoxyhydroquinone. Nine other proteins upregulated in SG-MS2 on exposure to (+)-pinoresinol appear to be homologs of proteins known to comprise the protocatechuate and 2-methoxyhydroquinone catabolic pathways, but only three of the cognate genes lie within the cluster containing the flavoprotein and cytochrome genes.

IMPORTANCE (+)-Pinoresinol is an important plant defense compound, a major food lignan for humans and some other animals, and the model compound used to study degradation of the β-β' linkages in lignin. We report a gene cluster, in one strain each of Pseudomonas and Burkholderia, that is involved in the oxidative catabolism of (+)-pinoresinol. The flavoprotein component of the α-hydroxylase which heads the pathway belongs to the 4-phenol oxidizing (4PO) subgroup of the vanillyl alcohol oxidase/p-cresol methyl hydroxylase (VAO/PCMH) enzyme family but constitutes a novel combination of cofactor and electron acceptor properties for the family. It is translationally coupled with a cytochrome gene whose product is also required for activity. The work casts new light on the biology of (+)-pinoresinol and its transformation to other bioactive molecules. Potential applications of the findings include new options for deconstructing lignin into useful chemicals and the generation of new phytoestrogenic enterolactones from lignans.





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Microsoft Office For Android Will Be Supported On Chrome OS

U.S. tech giants Microsoft and Google have partnered wherein Office for Android will be supported on Chrome OS-based devices via the Google Play Store.




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Google said to be preparing its own chips for use in Pixel phones and Chromebooks

Google is reportedly on the verge of stepping up their hardware game in a way that follows the example set by Apple, with custom-designed silicon powering future smartphones. Axios reports that Google is readying its own in-house processors for use in future Pixel devices, including both phones and eventually Chromebooks, too. Google’s efforts around its […]




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Tree planting search engine Ecosia is getting a visibility boost in Chrome

Ecosia, a not-for-profit search engine which uses ad generated revenue to fund planting trees, is set to get a visibility boost in Chrome. A change Google is making to its chromium engine will see it added as a default search engine choice in up to 47 markets for the version 81 release of Google’s web […]




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Bella Hadid and Kendall Jenner rock raunchy LBDs at Chrome Hearts bash

Bella wowed in a show-stopping look as she proved to be the life and soul of the bash - which was also attended by Cindy Crawford and Sara Sampaio.




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Leeds house is transformed into a unique monochrome home

The once humble three-bed detached home in Leeds was transformed into a remarkable residence after its owner gave it a makeover with bright white gloss.




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V Festival 2013: Jessie J wears SAME monochrome bralet and pant combination on 2nd day

Jessie J is not normally one to skimp on costume changes.




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Justin Bieber shares sultry snapshots of wife Hailey posing in a chrome bathtub while in quarantine

Justin Bieber gave fans a glimpse of his luxurious quarantine life, when he took to Instagram to share some sultry portraits he snapped of wife Hailey Bieber on Friday afternoon.




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Charlize Theron is magical in monochrome look at Birkenstock 1774 Collection Launch Party

Charlize Theron wore something a little more comfortable on her feet on Thursday night, when the 44-year-old donned Birkenstock sandals for the launch of the company's latest line.




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Keira Knightley PICTURE EXC: Heavily pregnant star displays her bump in monochrome maxi dress

The 34-year-old actress sported a full-length monochrome dress underneath a light blue denim jacket as she went shopping for fruit at a local green grocers.




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Tori Kelly looks magical in monochrome as she attends CMT's Artist Of The Year

Sometimes the best accessory is a husband dressed in all black, as music star Tori Kelly displayed on Wednesday at CMT's Artist of the Year event in Nashville, Tennessee.




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Zara Tindall gets the monochrome memo as she joins trend sporting black and white Cheltenham races

Wrapping up warm from the British spring, the Queen's eldest granddaughter, 38, wore a houndstooth, knee-length coat dress, which she paired with maroon accessories.




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Google may be developing own processor for powering its line of Pixel phones and Chromebook laptops

Google's development of a processor for Pixel phones and Chromebooks could materialize a chip as soon as early next year and could help the tech giant support on-board artificial intelligence.




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Vizio points to outdated Chromecast software as potential cause of streaming problems with Disney+

After connectivity issues with the Disney+ during its launch yesterday, Vizio has announced it's working on an update for its SmartCast TVs that could help some users access the service.




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चेतावनी! सारे काम छोड़ कर अभी अपडेट करें अपना Google Chrome, मंडरा रहा है खतरा

अपडेट करना इसलिए ज़रूरी है क्योंकि जब तक गूगल ने इस खामी को ट्रैक कर इसके लिए उपाय निकाला है, हैकर्स ने इसका फायदा उठा लिया है.




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Google Chrome: बिना इंटरनेट के अब ऑफलाइन कंटेंट पढ़ सकेंगे यूजर्स

क्रोम ब्राउजर अपडेट के जरिए यूजर्स कंटेंट को ऑफलाइन भी पढ़ सकेंगे.




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If You Haven’t Already, Microsoft Just Gave You Another Reason to Switch to Edge From Google Chrome

The automatic switching for profiles will arrive with Microsoft Edge 83, which is expected by mid-May