Cristina Chelmu-Voda

Dr. Cristina Chelmu-Voda


Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
5 February 2025 in Biomedicines
Verified
Journal Article
Open access
PDF file
CCCristina Chelmu-Voda
Cristina Chelmu-Voda
ISIoana Anca Stefanopol
Ioana Anca Stefanopol
GGGabriela Gurău
Gabriela Gurău
MHMaria Andrada Hincu
Maria Andrada Hincu
GPGabriel Valeriu Popa
Gabriel Valeriu Popa
MCMehedinti Mihaela Cezarina
Mehedinti Mihaela Cezarina
Background: Angiogenesis, the formation of new blood vessels from pre-existing ones, plays a pivotal role in wound healing, particularly in surgical contexts. Methods and results: However, this process can be significantly impaired in patients with childhood obesity, resulting in delayed healing and additional complications. The biological process of wound healing is complex, involving angiogenesis, cell proliferation, inflammation, and tissue remodeling. This review aims to explore recent advancements in research on angiogenesis in surgical wounds in patients with childhood obesity, with a focus on growth factors, inflammation, microcirculation, and innovative therapeutic strategies. Conclusions: It highlights therapeutic approaches such as the administration of growth factors and the application of biomaterials to enhance angiogenesis.

27 November 2025 in Biomedicines
Verified
Journal Article
Open access
PDF file
AOAndreea Onofrei
Andreea Onofrei
FMFelicia Mihailuta
Felicia Mihailuta
DMDaniela Mihalache
Daniela Mihalache
CCCristina Chelmu-Voda
Cristina Chelmu-Voda
SJSanda Jurja
Sanda Jurja
MMMihaela Cezarina Mehedinți
Mihaela Cezarina Mehedinți
Background/Objectives: Therapeutic resistance remains a major obstacle in breast cancer management, particularly among estrogen receptor-positive (ERα+) tumors that initially respond to endocrine therapy such as tamoxifen. Type XI collagen (COL11A1), a minor fibrillar collagen secreted by cancer-associated fibroblasts, has recently emerged as a stromal biomarker linked to tumor progression, immune modulation, and poor prognosis in several solid malignancies. Methods: We conducted a narrative review of the literature indexed in PubMed, Scopus, and Web of Science between 2011 and 2025, including original research, reviews, and clinical studies addressing COL11A1 expression and function in breast cancer. Mechanistic studies in other cancer types (ovarian, pancreatic, lung) were also evaluated when relevant to breast cancer biology. Results: Across multiple cancer types, COL11A1 overexpression correlates with stromal remodeling, epithelial–mesenchymal transition, and resistance to both hormone therapy and chemotherapy. In breast cancer, emerging data suggest a potential prognostic role and possible involvement in shaping the immune microenvironment. Nevertheless, most evidence derives from retrospective or preclinical studies, and clinical validation remains limited. Conclusions: COL11A1 represents a promising, though still exploratory, biomarker of therapeutic resistance and immune modulation in breast cancer. Future prospective and subtype-specific studies are needed to clarify its diagnostic and therapeutic value and to determine whether its inclusion in immunohistochemical panels could enhance patient stratification and guide personalized treatment.