Yang Lin, Feng Lv, Fangfang Liu
Objective:Pyruvatekinase M2 (PKM2) is the key enzyme
in Warburg effect and was reported to be involved in metabolic pathways of
tumor cells response to chemotherapeutic drugs recently. In this study, we
examined the correlation between the expression of PKM2 and the sensitivity of
primary breast cancer cells to anticancer drugs. Method: PKM2 expression
was studied by immunohistochemistry in 296 cases of invasive breast cancer
patients' biopsy, and all the patients had collagen gel droplet embedded
culture-drug sensitivity test (CD-DST) to detect in vitro chemosensitivity
after surgery. Result: We found high PKM2 expression significantly
associated with good sensitivity to epirubicin (EPI) (P=0.019) and
5-fluorouracil (5-Fu) (P=0.009). Then we used a small neoadjuvant
chemotherapy cases to confirm that the higher PKM2 expression, the better
pathological response to therapy was obtained in patients treated with EPI-based
or EPI plus 5-Fu chemotherapy regimens. Although univariate and multivariate
analysis indicated high PKM2 was a poor independent predictor of progression
free survival (PFS) (P=0.003) and overall survival (OS) (P=0.008)in
human breast cancer, in PKM2 high expression cohort alone patients received EPI-based
or EPI plus 5-Fu chemotherapy were found to have a favorable PFS (P=0.003,P=0.013) and OS (P=0.003, P=0.004) than non-EPI/5-Fu-based
treatment, respectively. Conclusion: Our findings confirmed the poor
prognosis of high PKM2 expression in breast cancer and revealed the predictive
value of PKM2 in therapeutic response to EPI and 5-Fu. Moreover, our results
provided the guidance of individual treatment for the patients with poor
prognosis prompted by high PKM2 expression.
Key
Words: breast cancer chemosensitivity PKM2
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