HMV-II

Cat.No.: CSC-C6251J

Species: Homo sapiens (Human)

Source: Vagina

Morphology: epithelial-like

Culture Properties: Adherent cells

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Cat.No.
CSC-C6251J
Description
Human cell line derived from melanotic melanoma (highly melanotic).
Species
Homo sapiens (Human)
Source
Vagina
Recommended Medium
Culture Properties
Adherent cells
Morphology
epithelial-like
Disease
Vaginal Melanoma
Storage and Shipping
Ship in dry ice.
Store in liquid nitrogen.
Synonyms
HMV-2; HMVII; Human Melanoma Vagina-II
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

HMV-II (IIIB) cell line is a human malignant melanoma cell line originally derived from a metastatic lesion. It is commonly used as an in vitro model of melanoma tumor progression. These cells are able to form adherent monolayer cultures and demonstrate fibroblast-like morphology. They are rapidly proliferating and show stable growth. HMV-II cells have been shown to express melanocytic markers such as tyrosinase and MITF. HMV-II melanoma cells show increased melanogenesis.

HMV-II cell lines express dysregulated pathways associated with cell cycle regulation, cell survival and cell migration which are commonly seen in malignant melanomas. This line has been used in research to study melanoma invasion and metastasis as well as resistance to anti-cancer drugs. Furthermore, HMV-II has been used to screen anti-cancer drugs such as targeted therapeutics and combination treatments.

Vaginal Mucosal Melanoma Cell Activation in Response to Photon or Carbon Ion Irradiation

Primary gynecological melanomas are rare and more lethal than cutaneous forms; whether mucosal melanocytes modulate radiosensitivity is unknown. Charalampopoulou et al. examined how photon vs carbon-ion irradiation affects morphology, melanogenesis and motility of human vaginal-mucosal HMV-II melanoma cells.

Under standard culture conditions, HMV-II melanoma cells maintained epithelial morphology with triangular or spindle-shaped bodies and short processes. Following XRT or CIRT exposure, cells exhibited dose- and radiation-type-dependent morphological activation characterized by dendrite formation and elongated morphology (Fig. 1a-c). After photon irradiation, average dendrite length increased progressively with dose, peaking at 6 Gy and declining at 8-10 Gy by 24 h; this morphology persisted for 10 days (Fig. 1d). Carbon ion irradiation produced less pronounced changes at 24 h, but dendrite elongation emerged by 48 h, similarly peaking at 6 Gy and maintaining this pattern through day 10 (Fig. 1e). Notably, XRT induced significantly greater dendrite elongation than CIRT at all time points (Fig. 1f).

Dendritic processes of HMV-II cells at (a) normal conditions (no exposure to irradiation) and after the exposure to 6 Gy of (b) C-ions and (c) photons, obtained using a phase-contrast microscope at 100X magnification. (d) Normalized data of dendrite length after the exposure to photons and to (e) C-ions. (f) Comparison of dendrite length between photons and C-ions at 2, 6, and 8 Gy.

Fig. 1. Dendritic processes of HMV-II cells at (a) normal conditions (no exposure to irradiation) and after the exposure to 6 Gy of (b) C-ions and (c) photons, obtained using a phase-contrast microscope at 100X magnification. (d) Normalized data of dendrite length after the exposure to photons and to (e) C-ions. (f) Comparison of dendrite length between photons and C-ions at 2, 6, and 8 Gy (Charalampopoulou A, Barcellini A, et al., 2024).

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