Publications by authors named "Monique Cadrin"

In Brief: The regulation of AKT in the endometrium during many cellular processes such as apoptosis and cell survival is crucial during the estrous cycle to ensure fertility. This research shows the specific function of AKT isoforms in the mouse endometrium for litter size, estrous cyclicity and endometrial gland development.

Abstract: Apoptosis and cell survival regulation are crucial processes during the estrous cycle to prepare a receptive uterus during implantation for successful recognition of pregnancy.

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Article Synopsis
  • The PI3K/Akt signaling pathway is often disrupted in cancer and is associated with uncontrolled cell growth; however, therapies targeting it alone have not been very effective.
  • This study highlights the potential benefits of combining PI3K/Akt inhibitors, specifically NVP-BEZ235 and AZD5363, with chemotherapeutic drugs like cisplatin and doxorubicin to enhance their effectiveness.
  • Results indicate that NVP-BEZ235 primarily enhances the effects of cisplatin, while AZD5363 increases sensitivity to doxorubicin, leading to increased apoptosis and reduced cancer cell proliferation when used together.
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Keratins 8 and 18 (K8/18) are simple epithelial cell-specific intermediate filament proteins. Keratins are essential for tissue integrity and are involved in intracellular signaling pathways that regulate cell response to injuries, cell growth, and death. K8/18 expression is maintained during tumorigenesis; hence, they are used as a diagnostic marker in tumor pathology.

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Akt/PKB kinases are central mediators of cell homeostasis. There are three highly homologous Akt isoforms, Akt1/PKBα, Akt2/PKBβ and Akt3/PKBγ. Hyperactivation of Akt signaling is a key node in the progression of a variety of human cancer, by modulating tumor growth, chemoresistance and cancer cell migration, invasion and metastasis.

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Keratins 8 and 18 (K8/18) intermediate filament proteins are believed to play an essential role in the protection of hepatocytes against mechanical and toxic stress. This assertion is mainly based on increased hepatocyte fragility observed in transgenic mice deficient in K8/18, or carrying mutations on K8/18. The molecular mechanism by which keratins accomplish their protective functions has not been totally elucidated.

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Keratin 8 and 18 are simple epithelial intermediate filament (IF) proteins, whose expression is differentiation- and tissue-specific, and is maintained during tumorigenesis. Vimentin IF is often co-expressed with keratins in cancer cells. Recently, IF have been proposed to be involved in signaling pathways regulating cell growth, death and motility.

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Frank B. Mallory described cytoplasmic hyaline inclusions in hepatocytes of patients with alcoholic hepatitis in 1911. These inclusions became known as Mallory bodies (MBs) and have since been associated with a variety of other liver diseases including non-alcoholic fatty liver disease.

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Article Synopsis
  • K20 is an intermediate filament protein found mainly in epithelial cells and is used to identify metastatic tumors, but its regulation and function were previously unclear.
  • Research shows that K20 is primarily phosphorylated at the Ser(13) site, which increases in response to protein kinase C activation and affects keratin filament organization.
  • Phosphorylation at Ser(13) is notably involved in cellular processes like apoptosis, tissue injury, and is also a specific marker for goblet cells in the small intestine.
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BACKGROUND: Keratins are members of the intermediate filaments (IFs) proteins, which constitute one of the three major cytoskeletal protein families. In hepatocytes, keratin 8 and 18 (K8/18) are believed to play a protective role against mechanical and toxic stress. Post-translational modifications such as phosphorylation and glycosylation are thought to modulate K8/18 functions.

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