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Tissue
硬腭、唾液腺
Disease
硬腭黏表皮样癌
Metastatic site
原发肿瘤部位(硬腭)
Synonyms
University of Michigan-Human Mucoepidermoid Carcinoma-3B

Documents

UM-HMC-3B

Cell line · Product number 305715

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01General information

Description

UM-HMC-3B 是一种人黏液表皮样癌细胞系,源自一名 73 岁白人女性患者硬腭唾液腺的原发性黏液表皮样癌。 该细胞系属于密歇根大学人类黏液表皮样癌(UM-HMC)细胞库的一部分。 与 UM-HMC-1 一样,UM-HMC-3B 携带 CRTC1-MAML2 基因融合(MECT1-MAML2),这是大多数黏液表皮样癌的致癌驱动基因,由 t(11;19)(q21;p13) 易位所致,并驱动 CREB 和 Notch 通路的激活。

UM-HMC-3B 适用于硬腭和唾液腺黏液表皮样癌生物学研究、CRTC1-MAML2 信号传导研究,以及与其他 UM-HMC 面板细胞系的比较分析。 结合 UM-HMC-1 和该系列的其他成员,UM-HMC-3B 有助于识别不同解剖部位、年龄和性别的黏表皮样癌中共同和不同的分子特征。它还适用于针对融合致癌蛋白及其下游 CREB/Notch 效应因子的药物敏感性检测。

Tissue
硬腭、唾液腺
Disease
硬腭黏表皮样癌
Metastatic site
原发肿瘤部位(硬腭)
Applications
唾液腺癌研究;CRTC1-MAML2融合基因生物学;硬腭黏膜上皮癌生物学;CREB/Notch信号通路;密歇根大学与霍奇金-马丁癌症中心(UM-HMC)联合研究;药物敏感性检测
Synonyms
  • University of Michigan-Human Mucoepidermoid Carcinoma-3B

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent
GMO status
Non-GMO
GMO status details
No genetic modification; somatic CRTC1-MAML2 fusion acquired during tumor development
Biosafety level
1

03Characteristics

Morphology
上皮样
Cell type
上皮细胞
Doubling time
约24至48小时

04Identifiers

Citation
UM-HMC-3B(Cytion 产品编号 305715)
NCBI TaxID
9606
Cellosaurus
CVCL_Y472

05Expression and susceptibility

Mutational profile
突变:基因融合,CRTC1 + HGNC,MAML2,名称=CRTC1-MAML2,MECT1-MAML2。

06Handling and culture

Culture medium
DMEM:Ham's F12(1:1),w: 3.1 g/L 葡萄糖,w: 2.5 mM L-谷氨酰胺,w: 15 mM HEPES,w: 0.5 mM 丙酮酸钠,w: 1.2 g/L NaHCO3(Cytion 文章编号 820400a)。
Incubation atmosphere

37°C, 5%CO2, 加湿环境。

Supplements
在培养基中添加 10% FBS
Dissociation reagent
Accutase
Subculturing
移除培养基,用不含钙和镁的PBS洗涤,加入Accutase覆盖细胞,在室温下孵育8–10分钟,用培养基重悬细胞,以300×g离心3分钟,弃去上清液,将细胞接种到新鲜培养基中。
Split ratio
1 到 5
Seeding density
2-4×10⁴/cm²
Fluid renewal
每 2 至 3 天
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

07Quality control and cryopreservation

Sterility

使用基于 PCR 的检测方法和基于发光的支原体检测方法排除支原体污染。

为确保没有细菌、真菌或酵母菌污染,每天都要对细胞培养物进行目视检查。

Freeze medium
我们使用完全生长培养基(包括 FBS)+10% DMSO 或 CM-1(Cytion 商品目录编号 800100)作为冷冻保存培养基,以获得足够的解冻后存活率,CM-1(Cytion 商品目录编号 800100)含有优化的渗透保护剂和代谢稳定剂,可提高恢复能力并减少冷冻引起的应激。
Storage conditions

如需长期保存,可将样品瓶放入气相液氮中,温度约为 -150 至 -196 ℃。在-80 °C下保存只能作为转入液氮前的短暂过渡。

Shipping conditions

冷冻保存的细胞系用干冰装运,并用经过验证的隔热包装和足够的制冷剂在整个运输过程中保持约 -78 °C 的温度。收到货后,应立即检查容器,并立即将小瓶转移到适当的储藏室。

08Donor

Donor age
73 年
Ethnicity
高加索人