Are you currently facing challenges in developing effective CAR T cell therapies for solid tumors, struggling with antigen specificity, or overcoming the immunosuppressive tumor microenvironment? Our carcinoma-specific CAR construction service helps you accelerate drug discovery and obtain highly potent, precisely targeted CAR constructs through advanced genetic engineering and comprehensive validation.
As a group of cancers, carcinoma usually starts from the skin and spreads to other organs of the body. It accounts for 90% of all cancers, which mostly occur in adults, with the DNA mutation as its main cause. Major subtypes include breast, prostate, colorectal, lung, cervical, melanoma, renal cell carcinoma, and adenocarcinomas. Common symptoms include lumps, skin discoloration, and pain. Although few strategies show effectiveness in carcinoma treatment, immunotherapy has shown great potential as a promising approach to treat carcinoma, such as CAR modified T cells or natural killer (NK) cells. Experts from Creative Biolabs can offer various CAR-T cell or NK cell construction services according to your request.
Fig.1 CAR-T cells can be engineered to trigger and enhance the endogenous tumor-specific immune response.1
Creative Biolabs' carcinoma-specific CAR construction service provides a comprehensive, end-to-end solution for developing highly effective Chimeric Antigen Receptors tailored to the unique complexities of solid tumors. We deliver meticulously designed and validated CAR constructs, functional CAR-T cells, and detailed data analyses, empowering your preclinical and clinical advancements. Our solutions are specifically engineered to address critical challenges such as tumor antigen heterogeneity, the immunosuppressive tumor microenvironment, and T cell persistence, offering a pathway to more potent and safer immunotherapies for carcinoma.
As a leading and reliable service provider, Creative Biolabs is well known worldwide for its breakthroughs in the CAR production system. Based on targeting carcinoma-specific antigens, our outstanding scientists have constructed diverse CAR-T cells or CAR NK cells targeting these antigens. In addition to these, Creative Biolabs can also customize the CAR product according to your special requirements.
Q1: What types of carcinomas can your service target?
A1: Creative Biolabs' Carcinoma-Specific CAR Construction Service is highly versatile. We have extensive experience targeting a wide range of carcinomas, including but not limited to renal cell carcinoma, melanoma, lung malignancy, colorectal cancer, prostate cancer, breast cancer, adenocarcinomas, and cervical carcinoma. We can work with both established and novel carcinoma-specific antigens.
Q2: How do you address the immunosuppressive tumor microenvironment (TME) in solid tumors?
A2: We address the challenging TME through advanced CAR designs, including "armored" CARs that are engineered to secrete cytokines or express dominant-negative receptors. These modifications help remodel the TME, enhance T cell persistence, and recruit endogenous immune cells, thereby improving CAR-T cell efficacy in hostile solid tumor environments.
Q3: Can you work with both human and mouse T cells for CAR construction?
A3: Yes, our service is equipped to handle both human and mouse T cells. We utilize appropriate viral vectors (lentiviral for human T cells and retroviral for mouse T cells) and optimized protocols for T-cell sorting, activation, and transduction to ensure successful CAR expression and functionality in both species.
At Creative Biolabs, we are committed to accelerating your journey from scientific concept to therapeutic reality in carcinoma treatment. Our carcinoma-specific CAR construction service combines unparalleled scientific expertise with cutting-edge technology, delivering precise, potent, and safe CAR constructs designed to overcome the unique challenges of solid tumors. Partner with us to transform your research into groundbreaking cancer immunotherapies.
"The 4th-generation armored CARs constructed by Creative Biolabs have greatly facilitated our studies on T cell persistence in the harsh tumor microenvironment. We observed remarkably sustained anti-tumor activity, which was a significant improvement compared to our previous constructs." - 2025, Prof. JS Pr
"Creative Biolabs' comprehensive workflow, from scFv selection to final CAR-T cell validation, has streamlined our research process. Their detailed quality control and consistent deliverables have been invaluable in accelerating our preclinical development." - 2025, Dr. Sh Kr
Based on a great number of experiments, we are confident our first-class CAR products can greatly accelerate your project process. Please feel free to contact us at any time.
| Associated malignancy | Target antigen | Receptor type | Product |
|---|---|---|---|
| Renal cell carcinoma (RCC) | Carbonic anhydrase IX (CAIX) | scFv-CD28-41BB-CD3ζ | CAR-MZ204 |
| CSPG4 | scFv-CD28-CD3ζ | CAR-LC134 | |
| G250 epitope | iRGD-scFv-CD28-41BB-CD3ζ | CAR-LC371 | |
| VEGFR-2 | scFv-CD28-41BB-CD3ζ | CAR-LC132 | |
| scFv-CD28-CD3ζ | CAR-LC133 | ||
| Melanoma | EGFR | VHH-CD28-41BB-CD3ζ | XS-0323-LX9 |
| scFv-CD28-CD3ζ | CAR-LC098 | ||
| scFv-CD28-41BB-CD3ζ | CAR-LC100 | ||
| Trop2 | scFv-CD28-41BB-CD3ζ | CAR-LC190 | |
| PD-L1 | PD1-41BB-CD3ζ | CAR-LC282 | |
| Cs-1 | scFv (SLAMF7)-CD28-41BB-CD3ζ/scFv (FN)-cMYCmu | CAR-LC365 | |
| BCMA | scFv-CD28-41BB-CD3ζ | CAR-T-3-L335-2BZ | |
| CS1 | scFv-CD28-OX40-CD3ζ | CAR-NK-3-M329-2XZ | |
| CSH1 | scFv-CD28-41BB-CD3ζ | CAR-T-3-L349-2BZ | |
| HMW-MAA | scFv-CD28-41BB-CD3ζ | CAR-T-3-M318-2BZ | |
| NY-ESO-1 | scFv-CD28-41BB-CD3ζ | CAR-T-3-M323-2BZ | |
| GD3 | scFv-CD28-41BB-CD3ζ | CAR-T-3-M317-2BZ | |
| MART-1(DMF5) | scFv-CD28-41BB-CD3ζ | CAR-T-3-M310-2BZ | |
| CD56 | scFv-CD28-41BB-CD3ζ | CAR-T-3-M312-2BZ | |
| gp100 | VHH-41BB-CD3ζ | CAR-T-2-M552-BZ | |
| Lung malignancy | Mesothelin | scFv-CD28-41BB-CD3ζ | CAR-LC054 |
| 7H-YB-Fluc-EF1a-scFv-41BB-CD3ζ | XS-0822-YF8720 | ||
| scFv-CD28-CD3ζ | CAR-LC024 | ||
| ALK | scFv-CD28-41BB-CD3ζ | CAR-LC103 | |
| Fibroblast activation protein (FAP) | scFv-41BB-CD3ζ | CAR-LC224 | |
| CD87 | scFv-41BB-CD3ζ-IL12 | CAR-LC265 | |
| Tissue factor | Protein-41BB-CD3ζ | CAR-LC288 | |
| TF | scFv-CD28-OX40-CD3ζ | CAR-T-3-L406-2XZ | |
| Colorectal cancer | CEA | scFv-CD28-41BB-CD3ζ | CAR-T-3-M314-2BZ |
| EGP-2 | scFv-CD28-41BB-CD3ζ | CAR-T-3-M316-2BZ | |
| TAG-72 | scFv-CD28-41BB-CD3ζ | CAR-T-3-M325-2BZ | |
| CD276 | scFv-CD28-CD3ζ | CAR-LC162 | |
| EpCAM | scFv-CD28-41BB-CD3ζ | CAR-LC181 | |
| HLA-A2-WT1DB126 | scFv-CD28-FcγR1γ | CAR-LC266 | |
| Prostate cancer | PSMA | 7H-YB-IL15 SA-EF1a-scFv-CD28-CD3ζ | XS-0822-YF9698 |
| PSCA | scFv-CD28-CD3ζ | CAR-MZ157 | |
| Breast cancer | CD8 | scFv-41BB-CD3ζ-IL12 | CAR-LC265 |
| ErbB2 | scFv-CD28-41BB-CD3ζ | CAR-T-3-L337-2BZ | |
| MUC1 | scFv-CD28-41BB-CD3ζ | CAR-T-3-M322-2BZ | |
| TEM8 | scFv-CD28-41BB-CD3ζ | CAR-T-3-L343-2BZ | |
| SSEA4 | scFv-41BB-CD3ζ | CAR-LC001 | |
| CD33 | scFv-CD28-CD3ζ | CAR-LC155 | |
| HER2 | scFv-41BB-CD3ζ | CAR-LC172 | |
| NY-BR-1 | scFv-CD28-41BB-CD3ζ | CAR-LC220 | |
| CD44 | scFv-CD28-CD3ζ | CAR-LC226 | |
| CD47 | scFv (CD47)-CD28-41BB-CD3ζ/scFv (TAZ)-TET2 | CAR-LC364 |
Reference
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All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.
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