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- W2085096689 endingPage "66" @default.
- W2085096689 startingPage "52" @default.
- W2085096689 abstract "The adipogenic origin-derived liposarcoma (LPS) family is the most common soft tissue sarcoma histological subtype. This group is composed of three categories as per the 2002 WHO guidelines: (1) well-differentiated and dedifferentiated liposarcoma (WDLPS/DDLPS); (2) myxoid and round cell liposarcoma (MLS and RCL); and (3) pleomorphic liposarcoma (PLS). While clustered together, these histological subtypes are widely diverse in their clinical, pathological, and molecular characteristics. In general, surgery still remains the mainstay of LPS therapy and the only approach offering the potential of cure. Effective therapeutic strategies for locally advanced and metastatic disease are currently lacking and are crucially needed. With the current gradually increasing knowledge of LPS genetic- and epigenetic-associated deregulations, the ultimate goal is to develop drugs that can specifically eliminate LPS cells while sparing normal tissues. This tumor-tailored target-orientated approach will hopefully result in a significant improvement in the outcome of patients suffering from these poor prognosis malignancies." @default.
- W2085096689 created "2016-06-24" @default.
- W2085096689 creator A5008558439 @default.
- W2085096689 creator A5022298756 @default.
- W2085096689 creator A5050445982 @default.
- W2085096689 creator A5065854516 @default.
- W2085096689 date "2011-02-01" @default.
- W2085096689 modified "2023-09-30" @default.
- W2085096689 title "New frontiers in the treatment of liposarcoma, a therapeutically resistant malignant cohort" @default.
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