Publications by authors named "M Stanislawowski"

Article Synopsis
  • Multiple myeloma (MM) is a type of cancer involving the uncontrolled growth of abnormal plasma cells and affects the bone tissue microenvironment.
  • Bone marrow adipose tissue (BMAT) plays a significant role in MM progression, influencing the cancer through various biological pathways, and obesity can exacerbate this by increasing BMAT mass and disrupting bone health.
  • Factors such as impaired fat metabolism and increased harmful substances from fat cells are linked to the progression of MM, prompting a thorough review of existing research on the connection between excess fat and the risk of developing this cancer.
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Objective: CD73 (ecto-5'-nucleotidase, NT5E), a cell-surface enzyme converting 5'-AMP to adenosine, is crucial for cancer progression. However, its role in the tumorigenesis process remains mostly obscure. We aimed to demonstrate CD73's role in breast cancer (BC) tumorigenesis through metabolic rewiring of fatty acid metabolism, a process recently indicated to be regulated by BC major prognostic markers, hormone receptors (HR) for estrogen (ER), and progesterone (PR).

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Article Synopsis
  • CAR-T cells are a type of T cell therapy that are genetically modified to treat certain blood cancers, especially when previous treatments have failed.
  • The review discusses how CAR-T cells are activated, their receptor structures, and compares the effectiveness of CAR-T therapies currently approved in the EU.
  • It also explores the future potential for CAR-T cell therapy in Poland, along with possible new research directions, including advancements in CAR-T and CAR-natural killer (NK) cell therapies.
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Purpose: l-arginine (L-arg) deficiency causes immunosuppression, but it is unknown if L-arg supplementation in colorectal cancer (CRC) patients restores immune system activity. Our objective was to investigate the effect of L-arg supplementation on the frequency of monocytic (M) and polymorphonuclear (PNM) myeloid-derived suppressor cells (M-MDSCs and PMN-MDSCs, respectively).

Methods: We enrolled 65 CRC patients (34 males, 31 females) aged 69 ​± ​10 years into a prospective, randomised, double-blind study.

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HtrA proteases regulate cellular homeostasis and cell death. Their dysfunctions have been correlated with oncogenesis and response to therapeutic treatment. We investigated the relation between HtrA1-3 expression and clinicopathological, and survival data, as well as the microsatellite status of tumors.

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