Upregulated Glucose Metabolism Correlates Inversely with CD8(+) T-cell Infiltration and Survival in Squamous Cell Carcinoma

Antibodies that block T-cell–regulatory checkpoints have recently emerged as a transformative approach to cancer treatment. However, the clinical efficacy of checkpoint blockade depends upon inherent tumor immunogenicity, with variation in infiltrating T cells contributing to differences in objective response rates. Here, we sought to understand the molecular correlates of tumor-infiltrating T lymphocytes (TIL) in squamous cell carcinoma (SCC), using a systems biologic approach to integrate publicly available omics datasets with histopathologic features. We provide evidence that links TIL abundance and therapeutic outcome to the regulation of tumor glycolysis by EGFR and HIF, both of which are attractive molecular targets for use in combination with immunotherapeutics

Renal cell carcinoma in end-stage renal disease: A retrospective study in patients from Hungary

Introduction: End-stage renal disease (ESRD) and acquired cystic kidney disease (ACKD) are known risk factors for renal cell carcinoma (RCC). Hereby, the clinicopathological features of RCCs developed in ESRD were investigated. Methods: A database consisting of 34 tumors from 31 patients with ESRD among 2 566 nephrectomy samples of RCC was built. The demographic, clinical, and follow-up data along with pathological parameters were analyzed. The RCCs were diagnosed according to the current WHO Classification of Urinary and Male Genital Tumors. Results: Twenty-two tumors developed in men and 12 in women, with a median age of 56 years (range: 27-75 years). The causes of ESRD were glomerulonephritis (n=7), hypertensive kidney disease (n=6), autosomal dominant polycystic kidney disease (n=6), chronic pyelonephritis (n=4), diabetic nephropathy (n=3), chemotherapy-induced nephropathy (n=1), and undetermined (n=4). ACKD complicated ESRD in 12 patients. The following histological subtypes were identified: clear cell RCC (n=19), papillary RCC (n=5), clear cell papillary tumor (n=5), ACKD RCC (n=3), and eosinophilic solid and cystic RCC (n=2). The median tumor size was 31 mm (range: 10-80 mm), and 32 tumors were confined to the kidney (pT1-pT2). There was no tumor-specific death during the period of this study. Progression was registered in one patient.Conclusion: In our cohort, the most common RCC subtype was clear cell RCC (55%), with a frequency that exceeded international data appreciably (14-25%). The incidence of clear cell papillary tumor and ACKD RCC (14.7% and 8.5%) was lower than data reported in the literature (30% and 40%). Our results indicate a favorable prognosis of RCC in ESRD

Induction of fibroblast senescence generates a non-fibrogenic myofibroblast phenotype that differentially impacts on cancer prognosis

Cancer-associated fibroblasts (CAF) remain a poorly characterized, heterogeneous cell population. Here we characterized two previously described tumor-promoting CAF sub-types, smooth muscle actin (SMA)-positive myofibroblasts and senescent fibroblasts, identifying a novel link between the two. Analysis of CAF cultured ex vivo, showed that senescent CAF are predominantly SMA-positive; this was confirmed by immunochemistry in head & neck (HNSCC) and esophageal (EAC) cancers. In vitro, we found that fibroblasts induced to senesce develop molecular, ultrastructural and contractile features typical of myofibroblasts and this is dependent on canonical TGF-? signaling. Similar to TGF-?1-generated myofibroblasts, these cells secrete soluble factors that promote tumor cell motility. However, RNA-sequencing revealed significant transcriptomic differences between the two SMA-positive CAF groups, particularly in genes associated with extracellular matrix (ECM) deposition and organization, which differentially promote tumor cell invasion. Notably, second harmonic generation imaging and bioinformatic analysis of SMA-positive human HNSCC and EAC showed that collagen fiber organization correlates with poor prognosis, indicating that heterogeneity within the SMA-positive CAF population differentially impacts on survival. These results show that non-fibrogenic, SMA-positive myofibroblasts can be directly generated through induction of fibroblast senescence and suggest that senescence and myofibroblast differentiation are closely linked processes

Az Omikron Computer Kft. vagyoni-, pénzügyi, jövedelmezőségi helyzetének elemzése 2006-2010-ig

Az Omikron Computer Kft. vagyoni-, pénzügyi, jövedelmezőségi helyzetének elemzése 2006-2010-igMscSzámvite

Magyarországi máktermesztés helyzete, egy konkrét cég pénzügyi elemzése alapján

Dolgozatomban a cég pénzügyi adatainak köszönhetően, 4 évre visszamenőleg (2016, 2017, 2018, 2019) egy pénzügyi elemzést végeztem a cég gazdálkodásáról, pénzügyi, vagyoni és jövedelmi helyzetéről, azokról az eredményekről a vállalkozást érintő problémákról. Ezen folyamatok meghatározásában a vállalkozás mérlegadatai nyújtottak segítséget. A pénzügyi elemzés olyan eljárások összessége, amely során a vállalkozás mérleg adatainak az eszköz és forrás, illetve eredmények nyújtanak segítséget a vállalkozás hatékonyságának, pénzügyi teljesítőképességének minősítésére, vizsgálatára. Fő célkitűzésem annak a meghatározása, hogy milyen pénzügyi, vagyoni, jövedelmi helyzet jellemző Magyarország egyik legnagyobb mák integrátor és kereskedő vállalkozására.BSc/BAVidékfejlesztési agrármérnökiK

Tumor-stromal interactions in pancreatic cancer

Pancreatic adenocarcinoma has one of the worse prognoses of any cancer with a 5-year survival of only 3%. Pancreatic cancer displays one of the most prominent stromal reactions of all tumors and it is evident that this is a key contributing factor to disease outcome. The tumor microenvironment of pancreatic cancer harbors a wide spectrum of cell types and a complex network of mechanisms which all serve to promote tumor progression. It is clear that the symbiotic relationship between pancreatic cancer cells and stellate cells is the chief factor creating this unique tumor milieu. Pancreatic stellate cells play critical roles in evasion of cancer cell apoptosis, invasion and metastases, angiogenesis, and promotion of an immunosuppressive environment, all key hallmarks of malignancy. Existing treatments for pancreatic cancer focus on targeting the cancer cells rather than the whole tumor, of which cancer cells represent a small proportion. It is now increasingly evident that research targeted towards the interactions between these cell types, ideally at an early stage of tumor development, is imperative in order to propel the way forward to more effective treatments

In vitro effect of bisphosphonates on oral keratinocytes and fibroblasts

IntroductionOsteonecrosis of the jaws is a potential complication of bisphosphonate therapy. The underlying mechanism(s) remain unclear. While most research has concentrated on the effects of bisphosphonates on osteoclast and osteoblast function, the disease is diagnosed and classified on the basis of mucosal breakdown, suggesting that oral soft tissues may be involved in its pathogenesis.AimsTo determine the effect of three different bisphosphonate drugs (aledronate, zoledronate and clodronate) on the function of oral keratinocytes and fibroblasts.MethodsHuman oral keratinocytes (OKF6) and fetal foreskin fibroblasts (HFFF2) were exposed to each drug at several concentrations and the effect on cell proliferation was assessed by counting the viable cells after different lengths of treatment. The effect on cell migration was examined using Transwell migration assays. An organotypic co-culture model using keratinocytes and fibroblasts, which recapitulates the morphology of the oral mucosa, was used to assess the effect of the drugs on epithelial stratification and differentiation.ResultsThe three bisphosphonates affected the viability and proliferation of OKF6 and HFFF2 cells at concentrations in keeping with their known relative in vitro potencies. There was no effect on cell migration or tissue architecture in organotypic cultures at subtoxic concentrations.DiscussionThe lack of effect of these drugs on cell migration below concentrations known to affect cell viability suggests that bisphosphonate related osteonecrosis is not caused through suppression of keratinocyte or fibroblast motility