TY - JOUR
T1 - Ulcerated Cutaneous Melanoma
T2 - A Review of the Clinical, Histologic, and Molecular Features Associated with a Clinically Aggressive Histologic Phenotype
AU - Barricklow, Zoe
AU - Di Vincenzo, Mallory J.
AU - Angell, Colin D.
AU - Carson, William E.
N1 - Funding Information:
This work was supported in part by Grant Number 5T32 CA933840 (to MJD) and Grant Number 1T32 GM139784-01A1 (to CDA) from the National Institute of Health, P30 CA016058, National Cancer Institute, Bethesda, MD to the Comprehensive Cancer Center, The Ohio State University, Columbus, OH, and the Pelotonia Institute of Immuno-oncology (PIIO) at The Ohio State University. This research was also supported by Award Number UM1CA186712 from the National Cancer Institute and The John B. and Jane T. McCoy Chair in Cancer Research Endowment.
Funding Information:
This work was supported in part by Grant Number 5T32 CA933840 (to MJD) and Grant Number 1T32 GM139784-01A1 (to CDA) from the National Institute of Health, P30 CA016058, National Cancer Institute, Bethesda, MD to the Comprehensive Cancer Center, The Ohio State University, Columbus, OH, and the Pelotonia Institute of Immunooncology (PIIO) at The Ohio State University. This research was also supported by Award Number UM1CA186712 from the National Cancer Institute and The John B. and Jane T. McCoy Chair in Cancer Research Endowment.
Publisher Copyright:
© 2022 Barricklow et al.
PY - 2022
Y1 - 2022
N2 - The presence of ulceration in melanoma is associated with poor clinical outcomes and is the third most powerful predictor of survival in the AJCC Melanoma Staging System after tumor thickness and mitotic activity. The aggressive biological behavior associated with ulceration has been hypothesized to be the result of an intrinsic biological attribute that favors dissemination and presents locally with the loss of epidermal integrity. Among the features of ulcerated melanoma, many show promise as potential prognostic tools, markers of differential immunogenicity and indicators of oncogenic drivers of invasion and metastasis. The incidence of ulcerated melanoma is greater in males, increases with age and with systemic inflammatory risk factors (diabetes, smoking, low vitamin D, elevated body mass index). Patients with ulcerated primary tumors seem to exclusively benefit from adjuvant interferon (IFN) therapy, which is likely the consequence of an altered tumor microenvironment. When ulceration is present, there is a higher density of macrophages and dendritic cells and enhanced expression of pro-inflammatory cytokines, such as IL-6. There is also an increased expression of proteins involved in tumor antigen presentation in ulcerated melanomas. Histologically, vascular density, vasculogenic mimicry and angiotropism are all significantly correlated with ulceration in melanoma. The presence of ulceration is associated with reduced protein expression of E-cadherin and PTEN and elevated levels of N-cadherin and the matrix metalloproteinases. Differential microRNA expression also holds promise as a potential prognostic biomarker of malignancy and disease spread within the setting of ulceration. However, the molecular and cellular differences associated with the ulcerated state are complex and further study will aid in determining how these differences can be harnessed to improve care for patients with melanoma.
AB - The presence of ulceration in melanoma is associated with poor clinical outcomes and is the third most powerful predictor of survival in the AJCC Melanoma Staging System after tumor thickness and mitotic activity. The aggressive biological behavior associated with ulceration has been hypothesized to be the result of an intrinsic biological attribute that favors dissemination and presents locally with the loss of epidermal integrity. Among the features of ulcerated melanoma, many show promise as potential prognostic tools, markers of differential immunogenicity and indicators of oncogenic drivers of invasion and metastasis. The incidence of ulcerated melanoma is greater in males, increases with age and with systemic inflammatory risk factors (diabetes, smoking, low vitamin D, elevated body mass index). Patients with ulcerated primary tumors seem to exclusively benefit from adjuvant interferon (IFN) therapy, which is likely the consequence of an altered tumor microenvironment. When ulceration is present, there is a higher density of macrophages and dendritic cells and enhanced expression of pro-inflammatory cytokines, such as IL-6. There is also an increased expression of proteins involved in tumor antigen presentation in ulcerated melanomas. Histologically, vascular density, vasculogenic mimicry and angiotropism are all significantly correlated with ulceration in melanoma. The presence of ulceration is associated with reduced protein expression of E-cadherin and PTEN and elevated levels of N-cadherin and the matrix metalloproteinases. Differential microRNA expression also holds promise as a potential prognostic biomarker of malignancy and disease spread within the setting of ulceration. However, the molecular and cellular differences associated with the ulcerated state are complex and further study will aid in determining how these differences can be harnessed to improve care for patients with melanoma.
KW - melanoma
KW - review
KW - treatment
KW - ulcerated
UR - http://www.scopus.com/inward/record.url?scp=85136967532&partnerID=8YFLogxK
U2 - 10.2147/CCID.S372287
DO - 10.2147/CCID.S372287
M3 - Review article
AN - SCOPUS:85136967532
SN - 1178-7015
VL - 15
SP - 1743
EP - 1757
JO - Clinical, Cosmetic and Investigational Dermatology
JF - Clinical, Cosmetic and Investigational Dermatology
ER -