mouse breast cancer cell line 4t1  (ATCC)

Journal: Advanced Science

Article Title: Self‐Assembling Peptide‐Adjuvant Conjugate (SaPAC) Platform for Precision Cancer Immunotherapy

doi: 10.1002/advs.77632

Figure Lengend Snippet: Synergistic antitumor efficacy of trivalent SaPAC‐4T1 vaccination combined with anti‐PD‐1 checkpoint blockade in orthotopic 4T1 TNBC. (A) Treatment timeline. (B) Representative endpoint tumors (day 16; scale bar, 10 mm). (C) Longitudinal tumor volumes ( n = 6–8 mice/group). (D) Terminal tumor volumes on day 15. (E,F) Individual tumor growth trajectories. Data are the mean ± SEM; significance was assessed by unpaired two‐tailed Student's t‐test ( * p <0.05, ** p <0.01, *** p <0.001 vs. mock + anti‐PD‐1).

Article Snippet: The DC2.4 cell line, mouse bladder cancer cell line MB49, mouse melanoma cell line B16F10, and the mouse breast cancer cell line 4T1 were purchased from ATCC.

Techniques: Two Tailed Test

Journal: Advanced Science

Article Title: Self‐Assembling Peptide‐Adjuvant Conjugate (SaPAC) Platform for Precision Cancer Immunotherapy

doi: 10.1002/advs.77632

Figure Lengend Snippet: Peptides, peptide‐adjuvant conjugates, and fluorescently labeled peptides used in this study. The antigen epitope, linker/self‐assembly residues, and 1V209‐conjugated lysines (K * ) are indicated in the sequence column.

Article Snippet: The DC2.4 cell line, mouse bladder cancer cell line MB49, mouse melanoma cell line B16F10, and the mouse breast cancer cell line 4T1 were purchased from ATCC.

Techniques: Labeling, Sequencing, Conjugation Assay

Journal: Cancers

Article Title: Therapeutically Engineering Exosomes to Target CD206+ M2 Macrophages to Prevent the Development of Primary Tumors and Distal Metastases in Breast Cancers

doi: 10.3390/cancers18101619

Figure Lengend Snippet: Differential biodistribution of exosomes and protein in 4T1 tumors (Balb/c mice): I-131-labeled control exosomes (HEK293 exo), anti-mouse CD206 antibody (CD206 Ab), fusion protein (fusion P) containing targeting peptide and Fc-mIgG2b, and engineered exosomes (Engi. Exo) carrying targeting peptide were administered IV into 4T1 breast cancer-bearing animals; SPECT images were obtained 3 h after administration. ( A ) SPECT images showed the distribution of the agents in the primary tumors (white circles) and lungs (yellow rectangular areas). White arrows show possible metastatic foci. Fusion protein and engineered exosomes accumulated in the primary and metastatic tumors. We used rainbow color to depict the activity of I-131. Blue is the lowest and red is the highest activity of I-131. ( B ) Randomly selected lung H&E staining showed multiple metastatic foci (black arrows). ( C ) Presence of numerous CD206+ cells is seen in tumors (green cells). n = 2–3 animals per group. Ab = antibody, Engi = engineered, Exo = exosomes, HE = Hematoxylin and Eosin, P = protein, SPECT = single-photon emission computed tomography, H = heart.

Article Snippet: Syngeneic, aggressive triple-negative breast cancer (TNBC) mouse cell lines 4T1 (for Balb/c mice, ATCC, Manassas, VA, USA) and AT3 (for C57BL/6, Millipore, Burlington, MA, USA) were obtained and maintained in the laboratory in Dulbecco’s Modified Eagle Medium (DMEM) (Corning, Corning, NY, USA) supplemented with 10% fetal bovine serum (FBS) (Nalgene-GIBCO, Rochester, NY, USA), sodium pyruvate (GIBCO, Grand Island, NY, USA), non-essential amino acids (GIBCO), sodium glutamate (GIBCO), and 100 U/mL penicillin and streptomycin (GIBCO).

Techniques: Labeling, Control, Single Photon Emission Computed Tomography, Activity Assay, Staining

Journal: Cancers

Article Title: Therapeutically Engineering Exosomes to Target CD206+ M2 Macrophages to Prevent the Development of Primary Tumors and Distal Metastases in Breast Cancers

doi: 10.3390/cancers18101619

Figure Lengend Snippet: Resected model of breast cancer (4T1 in Balb/c mice) and metastasis: Representative images from tumor-resected animals (two from each group). All the primary tumors were resected 11 days after tumor cell implantation, and the animals were followed up to 63 days after resection. The figure shows representative animals from the control (HEK293 ( left panel )) and engineered exosome-treated ( right panel ) groups. The animals treated with the control exosomes began showing local recurrence and lung metastasis (black arrows show local recurrence and multiple distal metastases) starting on day 28 post-resection. None of the animals that received the engineered exosomes to deplete CD206+ cells showed any recurrence or distal metastasis. It is noteworthy that a small leftover tumor (white arrow) in one of the engineered exosome-treated animals disappeared following therapy on subsequent bioluminescent imaging. n = 5 per group. Pre-Sur = pre surgery, POD = post-operative day.

Article Snippet: Syngeneic, aggressive triple-negative breast cancer (TNBC) mouse cell lines 4T1 (for Balb/c mice, ATCC, Manassas, VA, USA) and AT3 (for C57BL/6, Millipore, Burlington, MA, USA) were obtained and maintained in the laboratory in Dulbecco’s Modified Eagle Medium (DMEM) (Corning, Corning, NY, USA) supplemented with 10% fetal bovine serum (FBS) (Nalgene-GIBCO, Rochester, NY, USA), sodium pyruvate (GIBCO, Grand Island, NY, USA), non-essential amino acids (GIBCO), sodium glutamate (GIBCO), and 100 U/mL penicillin and streptomycin (GIBCO).

Techniques: Control, Imaging