Publications by authors named "K G Roemer"

An important hallmark of radiation dermatitis is the impairment of the mitotic ability of the stem/progenitor cells in the basal cell layers due to radiation-induced DNA damage, leading to suppressed cell renewal in the epidermis. However, this mechanism alone does not adequately explain the complex pathogenesis of radiation-induced skin injury. In this review, we summarize the latest findings on the complex pathogenesis of radiation dermatitis and correlate these with the clinical features of radiation-induced skin reactions.

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Article Synopsis
  • HPV8, a type of human papillomavirus linked to skin cancer, affects immune cell presence and inflammation in patients with epidermodysplasia verruciformis (EV).
  • The study found that HPV8 E6 significantly induces the chemokine CCL2, attracting monocytes and leading to a predominance of macrophages in the lesions, surpassing even pro-inflammatory cytokines like TNF-α.
  • Researchers highlighted a specific mechanism involving the C/EBPα/miR-203/p63 pathway in how HPV8 E6 influences CCL2 production, showing that HPV8's oncoproteins disrupt skin immune balance for viral persistence.
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Background: Increasing evidence points at an important physiological role of the timekeeping system, known as the circadian clock (CC), regulating not only our sleep-awake rhythm but additionally many other cellular processes in peripheral tissues. It was shown in various cell types that environmental stressors, including ultraviolet B radiation (UV-B), modulate the expression of genes that regulate the CC (CCGs) and that these CCGs modulate susceptibility for UV-B-induced cellular damage. It was the aim of this pilot study to gain further insights into the CCs' putative role for UV-B-induced photocarcinogenesis of skin cancer.

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Calculated intersegmental moments are commonly used in analyzing throwing movements. The inverse dynamics (ID) results can vary due to the chosen set of body segment inertia parameters (BSIP). A multitude of methods to determine BSIP sets are available.

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Triggering receptor expressed on myeloid cells 2 (TREM2) is suggested to hamper antitumor immune response in multiple cancers. However, the role of TREM2 in oral squamous cell carcinoma (OSCC) and its expression in tumor-associated macrophages (TAMs) are unknown. In this study, TREM2 expression was analyzed in the primary tumors and corresponding lymph-node metastases of OSCC patients via immunohistochemistry on tissue microarrays.

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