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Updated: Jul 31, 2026

Tissue Engineering of Tumor Stromal Microenvironment with Application to Cancer Cell Invasion
Published on: March 18, 2014
Dermatomyositis/polymyositis associated with internal malignancy: a consequence of how neoplasms alter generalized
Abstract:
The mechanism of dermatomyositis/polymyositis (DM/PM) is unknown. There are multiple probable trigger mechanisms. Internal malignancy is a specific trigger for some cases of DM/PM. It is known that there are marked changes in the extracellular matrix around tumors and that various fractions of depolymerized glycosaminoglycans enter the circulation. Circulating ECM fractions are known to incorporate in the extracellular matrix (ECM). Skin changes in DM include mucin formation, edema, and atrophy. These are not post inflammatory changes. These changes could be a consequence of the tumor's effect in the generalized ECM. Many factors influence ECM. Infections are another probable trigger for DM/PM. Infections induce extracellular matrix changes. It is likely that a role for infectious agents in DM/PM will eventually be defined. The drug D-penicillamine is also a trigger for DM/PM. Understanding the mechanism of any one trigger might aid in helping define other triggers. Four other cutaneous signs of internal malignancy can be explained by the mechanism used to explain DM/PM.
Insights
The mechanism of dermatomyositis/polymyositis (DM/PM) remains unclear, but internal malignancy may trigger it by altering the extracellular matrix (ECM). Understanding this ECM alteration could illuminate other DM/PM triggers and associated skin conditions.
Area of Science:
- Dermatology
- Immunology
- Oncology
Background:
- The underlying mechanisms driving dermatomyositis/polymyositis (DM/PM) are not fully understood.
- Internal malignancy is a recognized trigger for a subset of DM/PM cases.
- Tumors induce significant alterations in the extracellular matrix (ECM), releasing fractions that enter circulation.
Purpose of the Study:
- To explore the potential role of extracellular matrix (ECM) alterations in the pathogenesis of dermatomyositis/polymyositis (DM/PM).
- To investigate the connection between internal malignancy, ECM changes, and characteristic skin manifestations in DM/PM.
- To hypothesize a unifying mechanism for DM/PM triggers, including malignancy, infections, and drugs.
Main Methods:
- Review of existing literature on DM/PM pathogenesis, ECM composition, and tumor-associated changes.
- Analysis of the proposed mechanism involving circulating ECM fractions and their incorporation into dermal ECM.
- Correlation of proposed ECM alterations with observed skin changes in dermatomyositis (DM), such as mucin formation, edema, and atrophy.
Main Results:
- Internal malignancy triggers DM/PM through alterations in the extracellular matrix (ECM).
- Circulating depolymerized glycosaminoglycans from tumors may be incorporated into the generalized ECM.
- Skin changes in DM, including mucin deposition, edema, and atrophy, are hypothesized to result from these ECM alterations rather than being solely post-inflammatory.
Conclusions:
- The proposed mechanism involving ECM alterations offers a potential explanation for DM/PM triggered by internal malignancy.
- This understanding may elucidate the role of other triggers like infections and drugs in DM/PM.
- The mechanism could also explain other cutaneous signs associated with internal malignancy.
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