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D2.0R雌性BALB/c小鼠D2乳腺增生性肺泡结节肿瘤细胞株mouse) breast cancer cell liine BioVector NTCC®典型培养物保藏中心

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  • 货  号:NTCC®-D2.0
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NTCC® D2.0R细胞系(或称 D2OR,Cellosaurus登录号CVCL_0I88)是一种鼠源(小鼠)乳腺癌细胞模型,在癌症研究中被广泛用于研究肿瘤休眠和转移复发。它通常与相关的、高增殖性的D2A1细胞系进行比较研究。

主要特性与研究价值
  • 起源: D2.0R细胞源自雌性BALB/c小鼠的D2乳腺增生性肺泡结节肿瘤,但其建系来源的肿瘤不易形成自发性转移。

  • 表型: 它的特点是在特定的微环境(体内和体外)中表现出休眠或静止表型。这些细胞可以以单个非增殖细胞的状态长期存活,然后在特定条件下重新激活并形成转移灶。

  • TGF- β –mediated EMT decreases mammary branching of D2.OR cells. (A)... |  Download Scientific Diagram


  • 研究用途: 该细胞系对于研究控制肿瘤从休眠状态转变为侵袭性、增殖性转移生长的机制至关重要。研究人员利用它来探讨细胞外基质(ECM)成分(如I型胶原蛋白可诱导增殖)和免疫系统(如自然杀伤细胞在维持休眠中起关键作用)在调节休眠中的作用。

  • 休眠标志物: 休眠的D2.0R细胞通常表达较低水平的增殖标志物Ki-67、磷酸化ERK,而表达较高水平的p38以及休眠相关基因,如Cfh和Gas6。ERK/p38活性的比例被认为是判断细胞增殖或休眠状态的关键指标。

  • 培养条件: 在使用基底膜提取物(BME)基质的标准3D培养系统中,D2.0R细胞通常保持静止(休眠)状态,而D2A1细胞则会增殖。

D2.0R模型已证实,使用针对活跃增殖细胞的常规化疗可能会“放过”非分裂的休眠癌细胞,而这些细胞正是后期转移的根源。这强调了开发专门针对休眠细胞的治疗方法的重要性。自体吞噬(Autophagy,又称细胞自噬)被发现是促进休眠D2.0R细胞存活的关键机制之一。

The D2.0R cell line (also written as D2.0R or D2OR, Cellosaurus accession CVCL_0I88) is a murine (mouse) breast cancer cell line widely used in cancer research as a model for studying tumor dormancy and metastatic relapse. It is typically compared with the related, highly proliferative D2A1 cell line.
Key Characteristics
  • Origin: The D2.0R cells were derived from a D2 hyperplastic alveolar nodule mammary tumor in a female BALB/c mouse, but were established from a tumor that did not readily form spontaneous metastases.

  • Phenotype: They are characterized by a dormant or quiescent phenotype in certain microenvironments both in vivo and in vitro, meaning they can survive as solitary, non-proliferating cells for extended periods before potentially forming metastases.

  • Breast cancer dormancy is associated with a 4NG1 state and not senescence |  npj Breast Cancer

  • Research Use: This cell line is crucial for investigating the mechanisms that control the switch from a dormant state to aggressive, proliferative metastatic growth. Researchers use it to study the role of the extracellular matrix (ECM) composition (e.g., type I collagen induces proliferation) and the immune system (e.g., natural killer cells are key for maintaining dormancy) in regulating dormancy.

  • Dormancy Markers: Dormant D2.0R cells express specific markers such as low levels of the proliferation marker Ki-67, low levels of phosphorylated ERK, high levels of p38, and high levels of dormancy-related genes like Cfh and Gas6.

  • Culture Conditions: In a standard 3D culture system using a basement membrane extract (BME) matrix, D2.0R cells typically remain quiescent (dormant), while the D2A1 cells proliferate.

The D2.0R model has been instrumental in demonstrating that effectively targeting proliferating cells with chemotherapy may spare non-dividing cancer cells, which can give rise to late-developing metastases. This highlights the need for therapies that specifically target dormant cells.


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