The Association Between Radiation-Induced miR-208a, Cancer Recurrence and Death Risk in Patients with Non-Small Cell Lung Cancer

Wenjing Ji, Yanzhi Bi, Qian Zheng, Ruirui Sun, Kejun Dai Oncology Department, Changzhou Cancer Hospital, Changzhou City, Jiangsu Province, 213000, People’s Republic of ChinaCorrespondence: Kejun Dai, Oncology Department, Changzhou Cancer Hospital, No. 68 Honghe Road, Xinbei District, Changzhou City, Jiangsu Province, 213000, People’s Republic of China, Email [email protected]: Existing experimental evidence suggested that the miR-208a expression in tumor tissue from non-small cell lung cancer (NSCLC) was significantly high after radiotherapy in vitro and in vivo, indicating a potential role for predicting NSCLC progression or recurrence. However, its prognostic value has not been fully confirmed among patients with NSCLC.Aim: We explored the association of serum miR-208a level with adverse events including cancer recurrence and/or metastasis and cancer death during a follow-up for 36 months after radiotherapy.Methods: We identified the serum level of miR-208a from 46 patients before and after surgical treatment combined with radiotherapy in NSCLC patients. The association between serum miR-208a and risk for the cancer recurrence and/or metastasis and cancer death among these patients were examined by Kaplan-Meier and multivariable Cox analysis.Results: The comprehensive outcomes during the follow-up period for 3 years including cancer recurrence and/or cancer metastasis and cancer death were 13 (28.3%) and 8 (17.4%), respectively. Kaplan-Meier analysis suggested that a high serum miR-208a level after radiotherapy tended to have a higher rate of cancer recurrence and/or cancer metastasis and a higher risk of cancer death than those with a low level of serum miR-208a. Furthermore, our multivariable Cox analysis suggested that elevated serum miR-208a levels were associated with an increased risk for cancer recurrence and/or cancer metastasis (HR=7.5, 95% CI: 2.5– 24.9, P< 0.01) and cancer death risk (HR=5.3, 95% CI: 1.7– 18.5, P< 0.05) after age, gender, smoking, drinking and tumor node metastasis (TNM) stage were controlled for.Conclusion: This study further provided evidence that elevated serum miR-208a levels after radiotherapy were associated with a high risk for cancer recurrence and/or metastasis and death among NSCLC patients.Keywords: radiotherapy, non-small cell lung cancer, microRNAs, recurrence, death

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SHILAP Revista de lepidopterología
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2025-10-01
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MicroRNA in disease regulation
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article

The Association Between Radiation-Induced miR-208a, Cancer Recurrence and Death Risk in Patients with Non-Small Cell Lung Cancer

SHILAP Revista de lepidopterología
MicroRNA in disease regulation
article

The Association Between Radiation-Induced miR-208a, Cancer Recurrence and Death Risk in Patients with Non-Small Cell Lung Cancer

article en

Abstract

Wenjing Ji, Yanzhi Bi, Qian Zheng, Ruirui Sun, Kejun Dai Oncology Department, Changzhou Cancer Hospital, Changzhou City, Jiangsu Province, 213000, People’s Republic of ChinaCorrespondence: Kejun Dai, Oncology Department, Changzhou Cancer Hospital, No. 68 Honghe Road, Xinbei District, Changzhou City, Jiangsu Province, 213000, People’s Republic of China, Email [email protected]: Existing experimental evidence suggested that the miR-208a expression in tumor tissue from non-small cell lung cancer (NSCLC) was significantly high after radiotherapy in vitro and in vivo, indicating a potential role for predicting NSCLC progression or recurrence. However, its prognostic value has not been fully confirmed among patients with NSCLC.Aim: We explored the association of serum miR-208a level with adverse events including cancer recurrence and/or metastasis and cancer death during a follow-up for 36 months after radiotherapy.Methods: We identified the serum level of miR-208a from 46 patients before and after surgical treatment combined with radiotherapy in NSCLC patients. The association between serum miR-208a and risk for the cancer recurrence and/or metastasis and cancer death among these patients were examined by Kaplan-Meier and multivariable Cox analysis.Results: The comprehensive outcomes during the follow-up period for 3 years including cancer recurrence and/or cancer metastasis and cancer death were 13 (28.3%) and 8 (17.4%), respectively. Kaplan-Meier analysis suggested that a high serum miR-208a level after radiotherapy tended to have a higher rate of cancer recurrence and/or cancer metastasis and a higher risk of cancer death than those with a low level of serum miR-208a. Furthermore, our multivariable Cox analysis suggested that elevated serum miR-208a levels were associated with an increased risk for cancer recurrence and/or cancer metastasis (HR=7.5, 95% CI: 2.5– 24.9, P< 0.01) and cancer death risk (HR=5.3, 95% CI: 1.7– 18.5, P< 0.05) after age, gender, smoking, drinking and tumor node metastasis (TNM) stage were controlled for.Conclusion: This study further provided evidence that elevated serum miR-208a levels after radiotherapy were associated with a high risk for cancer recurrence and/or metastasis and death among NSCLC patients.Keywords: radiotherapy, non-small cell lung cancer, microRNAs, recurrence, death

SHILAP Revista de lepidopterología
Research Institute of Radio (RU)
Good health and well-being
Openalex Percentile: Top 39%
MicroRNA in disease regulation
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