Publications by authors named "Patricia Lorden"

Relapse remains a major challenge in the clinical management of acute myeloid leukemia (AML) and is driven by rare therapy-resistant leukemia stem cells (LSCs) that reside in specific bone marrow niches. Hypoxia signaling maintains cells in a quiescent and metabolically relaxed state, desensitizing them to chemotherapy. This suggests the hypothesis that hypoxia contributes to the chemoresistance of AML-LSCs and may represent a therapeutic target to sensitize AML-LSCs to chemotherapy.

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  • Palatine tonsils act as primary defenders in our immune system against diseases we inhale or ingest, and researchers created a detailed map of the human tonsil, analyzing over 556,000 cells using various techniques.
  • They discovered 121 distinct cell types, traced their development, and outlined how different immune functions are organized within the tonsils.
  • The study's findings included identifying specific cell subtypes and regulatory factors, validating their results with age-related changes, and connecting the findings to understanding certain lymphomas, enhancing our knowledge of immune responses.
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Around 30-40% of patients with colorectal cancer (CRC) undergoing curative resection of the primary tumour will develop metastases in the subsequent years. Therapies to prevent disease relapse remain an unmet medical need. Here we uncover the identity and features of the residual tumour cells responsible for CRC relapse.

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  • The study focuses on how the mammalian germline undergoes significant epigenetic changes during the development of eggs and sperm, emphasizing the importance of resetting the epigenome before passing genetic information to the next generation.
  • It specifically examines X-chromosome inactivation and reactivation dynamics in primordial germ cell-like cells (PGCLCs) derived from mouse embryonic stem cells and finds that these processes differ from those in somatic cells.
  • The research concludes that proper X-chromosome remodeling is crucial for female germ cell development, with any failures in X-inactivation or patterns of reactivation leading to reduced meiotic potential.
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The tumor immune microenvironment is a main contributor to cancer progression and a promising therapeutic target for oncology. However, immune microenvironments vary profoundly between patients, and biomarkers for prognosis and treatment response lack precision. A comprehensive compendium of tumor immune cells is required to pinpoint predictive cellular states and their spatial localization.

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Female fertility is inversely correlated with maternal age due to a depletion of the oocyte pool and a reduction in oocyte developmental competence. Few studies have addressed the effect of maternal age on the human mature oocyte (MII) transcriptome, which is established during oocyte growth and maturation, however, the pathways involved remain unclear. Here, we characterize and compare the transcriptomes of a large cohort of fully grown germinal vesicle stage (GV) and in vitro matured (IVM-MII) oocytes from women of varying reproductive age.

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Background & Aims: There are few validated biomarkers that can be used to predict outcomes for patients with colorectal cancer. Part of the challenge is the genetic and molecular heterogeneity of colorectal tumors not only among patients, but also within tumors. We have explored intratumor heterogeneity at the epigenetic level, due to its dynamic nature.

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Purpose: Autism spectrum disorders are associated with defects in social response and communication that often occur in the context of intellectual disability. Rett syndrome is one example in which epilepsy, motor impairment, and motor disturbance may co-occur. Mutations in histone demethylases are known to occur in several of these syndromes.

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