Cutaneous Squamous Cell Carcinoma: From Pathophysiology to Novel Therapeutic Approaches
Cutaneous squamous cell carcinoma (cSCC), a non-melanoma skin cancer, is a keratinocyte carcinoma representing one of the most common cancers with an increasing incidence. cSCC could be in situ (e.g., Bowen's disease) or an invasive form. A significant cSCC risk factor is advanced age, together...
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creator | Fania, Luca Didona, Dario Di Pietro, Francesca Romana Verkhovskaia, Sofia Morese, Roberto Paolino, Giovanni Donati, Michele Ricci, Francesca Coco, Valeria Ricci, Francesco Candi, Eleonora Abeni, Damiano Dellambra, Elena |
description | Cutaneous squamous cell carcinoma (cSCC), a non-melanoma skin cancer, is a keratinocyte carcinoma representing one of the most common cancers with an increasing incidence. cSCC could be in situ (e.g., Bowen's disease) or an invasive form. A significant cSCC risk factor is advanced age, together with cumulative sun exposure, fair skin, prolonged immunosuppression, and previous skin cancer diagnoses. Although most cSCCs can be treated by surgery, a fraction of them recur and metastasize, leading to death. cSCC could arise de novo or be the result of a progression of the actinic keratosis, an in situ carcinoma. The multistage process of cSCC development and progression is characterized by mutations in the genes involved in epidermal homeostasis and by several alterations, such as epigenetic modifications, viral infections, or microenvironmental changes. Thus, cSCC development is a gradual process with several histological- and pathological-defined stages. Dermoscopy and reflectance confocal microscopy enhanced the diagnostic accuracy of cSCC. Surgical excision is the first-line treatment for invasive cSCC. Moreover, radiotherapy may be considered as a primary treatment in patients not candidates for surgery. Extensive studies of cSCC pathogenic mechanisms identified several pharmaceutical targets and allowed the development of new systemic therapies, including immunotherapy with immune checkpoint inhibitors, such as Cemiplimab, and epidermal growth factor receptor inhibitors for metastatic and locally advanced cSCC. Furthermore, the implementation of prevention measures has been useful in patient management. |
doi_str_mv | 10.3390/biomedicines9020171 |
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A significant cSCC risk factor is advanced age, together with cumulative sun exposure, fair skin, prolonged immunosuppression, and previous skin cancer diagnoses. Although most cSCCs can be treated by surgery, a fraction of them recur and metastasize, leading to death. cSCC could arise de novo or be the result of a progression of the actinic keratosis, an in situ carcinoma. The multistage process of cSCC development and progression is characterized by mutations in the genes involved in epidermal homeostasis and by several alterations, such as epigenetic modifications, viral infections, or microenvironmental changes. Thus, cSCC development is a gradual process with several histological- and pathological-defined stages. Dermoscopy and reflectance confocal microscopy enhanced the diagnostic accuracy of cSCC. Surgical excision is the first-line treatment for invasive cSCC. Moreover, radiotherapy may be considered as a primary treatment in patients not candidates for surgery. Extensive studies of cSCC pathogenic mechanisms identified several pharmaceutical targets and allowed the development of new systemic therapies, including immunotherapy with immune checkpoint inhibitors, such as Cemiplimab, and epidermal growth factor receptor inhibitors for metastatic and locally advanced cSCC. Furthermore, the implementation of prevention measures has been useful in patient management.</description><identifier>ISSN: 2227-9059</identifier><identifier>EISSN: 2227-9059</identifier><identifier>DOI: 10.3390/biomedicines9020171</identifier><identifier>PMID: 33572373</identifier><language>eng</language><publisher>BASEL: Mdpi</publisher><subject><![CDATA[Biochemistry & Molecular Biology ; Cancer therapies ; Confocal microscopy ; dermoscopy ; Disease ; Epidemiology ; Epidermal growth factor ; Epigenetics ; Homeostasis ; Human papillomavirus ; Immune checkpoint inhibitors ; Immunosuppression ; Immunotherapy ; Invasiveness ; keratinocyte carcinoma ; Keratosis ; Kinases ; Life Sciences & Biomedicine ; Males ; Medical prognosis ; Medical screening ; Medicine, Research & Experimental ; Melanoma ; Metastases ; Metastasis ; non-melanoma skin cancer ; Older people ; Pathophysiology ; Patients ; Pharmacology & Pharmacy ; Radiation therapy ; radiotherapy ; Research & Experimental Medicine ; Review ; Risk factors ; Science & Technology ; Skin cancer ; Squamous cell carcinoma ; Surgery ; therapy ; Ulcers ; Ultraviolet radiation ; Viral infections]]></subject><ispartof>Biomedicines, 2021-02, Vol.9 (2), p.171, Article 171</ispartof><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>126</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000622167000001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c565t-b01202dc1e7b604869d22ce5e6ebe94f98dda0e66a9d44fad2d8b1e369d37ef3</citedby><cites>FETCH-LOGICAL-c565t-b01202dc1e7b604869d22ce5e6ebe94f98dda0e66a9d44fad2d8b1e369d37ef3</cites><orcidid>0000-0002-3032-2217 ; 0000-0002-6779-8753 ; 0000-0002-4329-3312 ; 0000-0002-6119-1870 ; 0000-0002-7665-5471</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916193/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916193/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2115,27929,27930,39263,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33572373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fania, Luca</creatorcontrib><creatorcontrib>Didona, Dario</creatorcontrib><creatorcontrib>Di Pietro, Francesca Romana</creatorcontrib><creatorcontrib>Verkhovskaia, Sofia</creatorcontrib><creatorcontrib>Morese, Roberto</creatorcontrib><creatorcontrib>Paolino, Giovanni</creatorcontrib><creatorcontrib>Donati, Michele</creatorcontrib><creatorcontrib>Ricci, Francesca</creatorcontrib><creatorcontrib>Coco, Valeria</creatorcontrib><creatorcontrib>Ricci, Francesco</creatorcontrib><creatorcontrib>Candi, Eleonora</creatorcontrib><creatorcontrib>Abeni, Damiano</creatorcontrib><creatorcontrib>Dellambra, Elena</creatorcontrib><title>Cutaneous Squamous Cell Carcinoma: From Pathophysiology to Novel Therapeutic Approaches</title><title>Biomedicines</title><addtitle>BIOMEDICINES</addtitle><addtitle>Biomedicines</addtitle><description>Cutaneous squamous cell carcinoma (cSCC), a non-melanoma skin cancer, is a keratinocyte carcinoma representing one of the most common cancers with an increasing incidence. cSCC could be in situ (e.g., Bowen's disease) or an invasive form. 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Extensive studies of cSCC pathogenic mechanisms identified several pharmaceutical targets and allowed the development of new systemic therapies, including immunotherapy with immune checkpoint inhibitors, such as Cemiplimab, and epidermal growth factor receptor inhibitors for metastatic and locally advanced cSCC. Furthermore, the implementation of prevention measures has been useful in patient management.</description><subject>Biochemistry & Molecular Biology</subject><subject>Cancer therapies</subject><subject>Confocal microscopy</subject><subject>dermoscopy</subject><subject>Disease</subject><subject>Epidemiology</subject><subject>Epidermal growth factor</subject><subject>Epigenetics</subject><subject>Homeostasis</subject><subject>Human papillomavirus</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunosuppression</subject><subject>Immunotherapy</subject><subject>Invasiveness</subject><subject>keratinocyte carcinoma</subject><subject>Keratosis</subject><subject>Kinases</subject><subject>Life Sciences & Biomedicine</subject><subject>Males</subject><subject>Medical prognosis</subject><subject>Medical screening</subject><subject>Medicine, Research & Experimental</subject><subject>Melanoma</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>non-melanoma 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Approaches</atitle><jtitle>Biomedicines</jtitle><stitle>BIOMEDICINES</stitle><addtitle>Biomedicines</addtitle><date>2021-02-09</date><risdate>2021</risdate><volume>9</volume><issue>2</issue><spage>171</spage><pages>171-</pages><artnum>171</artnum><issn>2227-9059</issn><eissn>2227-9059</eissn><abstract>Cutaneous squamous cell carcinoma (cSCC), a non-melanoma skin cancer, is a keratinocyte carcinoma representing one of the most common cancers with an increasing incidence. cSCC could be in situ (e.g., Bowen's disease) or an invasive form. A significant cSCC risk factor is advanced age, together with cumulative sun exposure, fair skin, prolonged immunosuppression, and previous skin cancer diagnoses. Although most cSCCs can be treated by surgery, a fraction of them recur and metastasize, leading to death. cSCC could arise de novo or be the result of a progression of the actinic keratosis, an in situ carcinoma. The multistage process of cSCC development and progression is characterized by mutations in the genes involved in epidermal homeostasis and by several alterations, such as epigenetic modifications, viral infections, or microenvironmental changes. Thus, cSCC development is a gradual process with several histological- and pathological-defined stages. Dermoscopy and reflectance confocal microscopy enhanced the diagnostic accuracy of cSCC. Surgical excision is the first-line treatment for invasive cSCC. Moreover, radiotherapy may be considered as a primary treatment in patients not candidates for surgery. Extensive studies of cSCC pathogenic mechanisms identified several pharmaceutical targets and allowed the development of new systemic therapies, including immunotherapy with immune checkpoint inhibitors, such as Cemiplimab, and epidermal growth factor receptor inhibitors for metastatic and locally advanced cSCC. Furthermore, the implementation of prevention measures has been useful in patient management.</abstract><cop>BASEL</cop><pub>Mdpi</pub><pmid>33572373</pmid><doi>10.3390/biomedicines9020171</doi><tpages>33</tpages><orcidid>https://orcid.org/0000-0002-3032-2217</orcidid><orcidid>https://orcid.org/0000-0002-6779-8753</orcidid><orcidid>https://orcid.org/0000-0002-4329-3312</orcidid><orcidid>https://orcid.org/0000-0002-6119-1870</orcidid><orcidid>https://orcid.org/0000-0002-7665-5471</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry & Molecular Biology Cancer therapies Confocal microscopy dermoscopy Disease Epidemiology Epidermal growth factor Epigenetics Homeostasis Human papillomavirus Immune checkpoint inhibitors Immunosuppression Immunotherapy Invasiveness keratinocyte carcinoma Keratosis Kinases Life Sciences & Biomedicine Males Medical prognosis Medical screening Medicine, Research & Experimental Melanoma Metastases Metastasis non-melanoma skin cancer Older people Pathophysiology Patients Pharmacology & Pharmacy Radiation therapy radiotherapy Research & Experimental Medicine Review Risk factors Science & Technology Skin cancer Squamous cell carcinoma Surgery therapy Ulcers Ultraviolet radiation Viral infections |
title | Cutaneous Squamous Cell Carcinoma: From Pathophysiology to Novel Therapeutic Approaches |
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