Proteins, the primary building blocks of the cell membrane, play crucial roles in communication between cells as well as interactions with the extracellular matrix. They make for an excellent resource for disease identification due to their potential as biomarkers. In order to perform the study, HEL-299 (CCL-137™) and NCI-H209 lung cells were incubated at 37°C in a chamber that contained 5% CO2. Trypsinization was used to transfer the cells into Eppendorf tubes. Proteomics analyses were carried out using LC-QTOF equipment, and the corresponding procedures of denaturation, alkynylation, trypsinization, and purification were carried out by adding the required chemicals. The Searchquie and PeptideShacker software interfaces were used to assess the analysis findings. Proteins that differ across groups are displayed by classifying them based on their roles as cellular components, molecular activities, and biological processes. Proteomics data showed that the lung cancer cell line NCI-H209 lacked 14 proteins that were present in the healthy lung cell HEL-299. These are the proteins ANK3, PIK3R2, INPP5F, HSF1, VIM, NFAM1, SHROOM3, ETV4, RNF31, LMNA, BRD8, PRTN3, TERT, SMAD9. There were discovered to be 5 distinct proteins in the lung cancer group compared to healthy lung HEL-299 cells. These proteins are AHSG, NCOA6, VCP, DNAJC19, NCL. Given the heterogeneity of lung cancer, a thorough and in-depth investigation of lung cancer proteome profiling is necessary for effective target treatment. The examination of proteins as prospective lung cancer biomarker candidates shows that it will make up a viable source for clinical investigations. These proteins differ in the direction in this study. Potential clinical applications of the biomarkers identified in this study, such as early diagnosis, monitoring treatment response, and determining disease prognosis, may contribute to the development of personalized medicine approaches.
The development, acquisition, authentication, cryopreservation, and transfer of cell lines between laboratories were followed according to the guidelines published in the British Journal of Cancer, 2014.
Proteins, the primary building blocks of the cell membrane, play crucial roles in communication between cells as well as interactions with the extracellular matrix. They make for an excellent resource for disease identification due to their potential as biomarkers. In order to perform the study, HEL-299 (CCL-137™) and NCI-H209 lung cells were incubated at 37°C in a chamber that contained 5% CO2. Trypsinization was used to transfer the cells into Eppendorf tubes. Proteomics analyses were carried out using LC-QTOF equipment, and the corresponding procedures of denaturation, alkynylation, trypsinization, and purification were carried out by adding the required chemicals. The Searchquie and PeptideShacker software interfaces were used to assess the analysis findings. Proteins that differ across groups are displayed by classifying them based on their roles as cellular components, molecular activities, and biological processes. Proteomics data showed that the lung cancer cell line NCI-H209 lacked 14 proteins that were present in the healthy lung cell HEL-299. These are the proteins ANK3, PIK3R2, INPP5F, HSF1, VIM, NFAM1, SHROOM3, ETV4, RNF31, LMNA, BRD8, PRTN3, TERT, SMAD9. There were discovered to be 5 distinct proteins in the lung cancer group compared to healthy lung HEL-299 cells. These proteins are AHSG, NCOA6, VCP, DNAJC19, NCL. Given the heterogeneity of lung cancer, a thorough and in-depth investigation of lung cancer proteome profiling is necessary for effective target treatment. The examination of proteins as prospective lung cancer biomarker candidates shows that it will make up a viable source for clinical investigations. These proteins differ in the direction in this study. Potential clinical applications of the biomarkers identified in this study, such as early diagnosis, monitoring treatment response, and determining disease prognosis, may contribute to the development of personalized medicine approaches.
The development, acquisition, authentication, cryopreservation, and transfer of cell lines between laboratories were followed according to the guidelines published in the British Journal of Cancer, 2014.
Birincil Dil | İngilizce |
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Konular | Proteomik ve Metabolomik, Hücre Gelişimi, Proliferasyon ve Ölümü |
Bölüm | Araştırma Makaleleri |
Yazarlar | |
Yayımlanma Tarihi | 30 Aralık 2024 |
Gönderilme Tarihi | 5 Temmuz 2024 |
Kabul Tarihi | 5 Ekim 2024 |
Yayımlandığı Sayı | Yıl 2024 |
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